---
_id: '14253'
abstract:
- lang: eng
  text: Junctions between the endoplasmic reticulum (ER) and the plasma membrane (PM)
    are specialized membrane contacts ubiquitous in eukaryotic cells. Concentration
    of intracellular signaling machinery near ER-PM junctions allows these domains
    to serve critical roles in lipid and Ca2+ signaling and homeostasis. Subcellular
    compartmentalization of protein kinase A (PKA) signaling also regulates essential
    cellular functions, however, no specific association between PKA and ER-PM junctional
    domains is known. Here, we show that in brain neurons type I PKA is directed to
    Kv2.1 channel-dependent ER-PM junctional domains via SPHKAP, a type I PKA-specific
    anchoring protein. SPHKAP association with type I PKA regulatory subunit RI and
    ER-resident VAP proteins results in the concentration of type I PKA between stacked
    ER cisternae associated with ER-PM junctions. This ER-associated PKA signalosome
    enables reciprocal regulation between PKA and Ca2+ signaling machinery to support
    Ca2+ influx and excitation-transcription coupling. These data reveal that neuronal
    ER-PM junctions support a receptor-independent form of PKA signaling driven by
    membrane depolarization and intracellular Ca2+, allowing conversion of information
    encoded in electrical signals into biochemical changes universally recognized
    throughout the cell.
acknowledgement: We thank Kayla Templeton and Peter Turcanu for technical assistance,
  Michelle Salemi for assistance with LC-MS data acquisition and analysis, Dr. Belvin
  Gong for advice on monoclonal antibody generation, Drs. Maria Casas Prat and Eamonn
  Dickson for assistance with super-resolution TIRF microscopy, Dr. Oscar Cerda for
  assistance with the design of TAT-FFAT peptides, Dr. Fernando Santana for helpful
  discussions, and Dr. Jodi Nunnari for a careful reading of our manuscript. We also
  thank Dr. Alan Howe, Dr. Sohum Mehta, and Dr. Jin Zhang for providing plasmids used
  in this study. This project was funded by NIH Grants R01NS114210 and R21NS101648
  (J.S.T.), and F32NS108519 (N.C.V.).
article_number: '5231'
article_processing_charge: Yes
article_type: original
author:
- first_name: Nicholas C.
  full_name: Vierra, Nicholas C.
  last_name: Vierra
- first_name: Luisa
  full_name: Ribeiro-Silva, Luisa
  last_name: Ribeiro-Silva
- first_name: Michael
  full_name: Kirmiz, Michael
  last_name: Kirmiz
- first_name: Deborah
  full_name: Van Der List, Deborah
  last_name: Van Der List
- first_name: Pradeep
  full_name: Bhandari, Pradeep
  id: 45EDD1BC-F248-11E8-B48F-1D18A9856A87
  last_name: Bhandari
  orcid: 0000-0003-0863-4481
- first_name: Olivia A.
  full_name: Mack, Olivia A.
  last_name: Mack
- first_name: James
  full_name: Carroll, James
  last_name: Carroll
- first_name: Elodie
  full_name: Le Monnier, Elodie
  id: 3B59276A-F248-11E8-B48F-1D18A9856A87
  last_name: Le Monnier
- first_name: Sue A.
  full_name: Aicher, Sue A.
  last_name: Aicher
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: James S.
  full_name: Trimmer, James S.
  last_name: Trimmer
citation:
  ama: Vierra NC, Ribeiro-Silva L, Kirmiz M, et al. Neuronal ER-plasma membrane junctions
    couple excitation to Ca2+-activated PKA signaling. <i>Nature Communications</i>.
    2023;14. doi:<a href="https://doi.org/10.1038/s41467-023-40930-6">10.1038/s41467-023-40930-6</a>
  apa: Vierra, N. C., Ribeiro-Silva, L., Kirmiz, M., Van Der List, D., Bhandari, P.,
    Mack, O. A., … Trimmer, J. S. (2023). Neuronal ER-plasma membrane junctions couple
    excitation to Ca2+-activated PKA signaling. <i>Nature Communications</i>. Springer
    Nature. <a href="https://doi.org/10.1038/s41467-023-40930-6">https://doi.org/10.1038/s41467-023-40930-6</a>
  chicago: Vierra, Nicholas C., Luisa Ribeiro-Silva, Michael Kirmiz, Deborah Van Der
    List, Pradeep Bhandari, Olivia A. Mack, James Carroll, et al. “Neuronal ER-Plasma
    Membrane Junctions Couple Excitation to Ca2+-Activated PKA Signaling.” <i>Nature
    Communications</i>. Springer Nature, 2023. <a href="https://doi.org/10.1038/s41467-023-40930-6">https://doi.org/10.1038/s41467-023-40930-6</a>.
  ieee: N. C. Vierra <i>et al.</i>, “Neuronal ER-plasma membrane junctions couple
    excitation to Ca2+-activated PKA signaling,” <i>Nature Communications</i>, vol.
    14. Springer Nature, 2023.
  ista: Vierra NC, Ribeiro-Silva L, Kirmiz M, Van Der List D, Bhandari P, Mack OA,
    Carroll J, Le Monnier E, Aicher SA, Shigemoto R, Trimmer JS. 2023. Neuronal ER-plasma
    membrane junctions couple excitation to Ca2+-activated PKA signaling. Nature Communications.
    14, 5231.
  mla: Vierra, Nicholas C., et al. “Neuronal ER-Plasma Membrane Junctions Couple Excitation
    to Ca2+-Activated PKA Signaling.” <i>Nature Communications</i>, vol. 14, 5231,
    Springer Nature, 2023, doi:<a href="https://doi.org/10.1038/s41467-023-40930-6">10.1038/s41467-023-40930-6</a>.
  short: N.C. Vierra, L. Ribeiro-Silva, M. Kirmiz, D. Van Der List, P. Bhandari, O.A.
    Mack, J. Carroll, E. Le Monnier, S.A. Aicher, R. Shigemoto, J.S. Trimmer, Nature
    Communications 14 (2023).
date_created: 2023-09-03T22:01:14Z
date_published: 2023-08-26T00:00:00Z
date_updated: 2025-09-09T12:50:49Z
day: '26'
ddc:
- '570'
department:
- _id: RySh
doi: 10.1038/s41467-023-40930-6
external_id:
  isi:
  - '001064563400013'
  pmid:
  - '37633939'
file:
- access_level: open_access
  checksum: 6ab8aab4e957f626a09a1c73db3388fb
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T06:50:07Z
  date_updated: 2023-09-06T06:50:07Z
  file_id: '14270'
  file_name: 2023_NatureComm_Vierra.pdf
  file_size: 9412549
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T06:50:07Z
has_accepted_license: '1'
intvolume: '        14'
isi: 1
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
publication: Nature Communications
publication_identifier:
  eissn:
  - 2041-1723
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Neuronal ER-plasma membrane junctions couple excitation to Ca2+-activated PKA
  signaling
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 14
year: '2023'
...
---
_id: '14254'
abstract:
- lang: eng
  text: In [10] Nam proved a Lieb–Thirring Inequality for the kinetic energy of a
    fermionic quantum system, with almost optimal (semi-classical) constant and a
    gradient correction term. We present a stronger version of this inequality, with
    a much simplified proof. As a corollary we obtain a simple proof of the original
    Lieb–Thirring inequality.
acknowledgement: J.P.S. thanks the Institute of Science and Technology Austria for
  the hospitality and support during a visit where this work was done. J.P.S. was
  also partially supported by the VILLUM Centre of Excellence for the Mathematics
  of Quantum Theory (QMATH) (grant No. 10059).
article_number: '110129'
article_processing_charge: Yes (via OA deal)
article_type: original
arxiv: 1
author:
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
- first_name: Jan Philip
  full_name: Solovej, Jan Philip
  last_name: Solovej
citation:
  ama: Seiringer R, Solovej JP. A simple approach to Lieb-Thirring type inequalities.
    <i>Journal of Functional Analysis</i>. 2023;285(10). doi:<a href="https://doi.org/10.1016/j.jfa.2023.110129">10.1016/j.jfa.2023.110129</a>
  apa: Seiringer, R., &#38; Solovej, J. P. (2023). A simple approach to Lieb-Thirring
    type inequalities. <i>Journal of Functional Analysis</i>. Elsevier. <a href="https://doi.org/10.1016/j.jfa.2023.110129">https://doi.org/10.1016/j.jfa.2023.110129</a>
  chicago: Seiringer, Robert, and Jan Philip Solovej. “A Simple Approach to Lieb-Thirring
    Type Inequalities.” <i>Journal of Functional Analysis</i>. Elsevier, 2023. <a
    href="https://doi.org/10.1016/j.jfa.2023.110129">https://doi.org/10.1016/j.jfa.2023.110129</a>.
  ieee: R. Seiringer and J. P. Solovej, “A simple approach to Lieb-Thirring type inequalities,”
    <i>Journal of Functional Analysis</i>, vol. 285, no. 10. Elsevier, 2023.
  ista: Seiringer R, Solovej JP. 2023. A simple approach to Lieb-Thirring type inequalities.
    Journal of Functional Analysis. 285(10), 110129.
  mla: Seiringer, Robert, and Jan Philip Solovej. “A Simple Approach to Lieb-Thirring
    Type Inequalities.” <i>Journal of Functional Analysis</i>, vol. 285, no. 10, 110129,
    Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.jfa.2023.110129">10.1016/j.jfa.2023.110129</a>.
  short: R. Seiringer, J.P. Solovej, Journal of Functional Analysis 285 (2023).
corr_author: '1'
date_created: 2023-09-03T22:01:14Z
date_published: 2023-11-15T00:00:00Z
date_updated: 2024-10-09T21:06:47Z
day: '15'
ddc:
- '510'
department:
- _id: RoSe
doi: 10.1016/j.jfa.2023.110129
external_id:
  arxiv:
  - '2303.04504'
  isi:
  - '001071552300001'
file:
- access_level: open_access
  checksum: 28e424ad91be6219e9d321054ce3a412
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-30T14:15:16Z
  date_updated: 2024-01-30T14:15:16Z
  file_id: '14915'
  file_name: 2023_JourFunctionalAnalysis_Seiringer.pdf
  file_size: 232934
  relation: main_file
  success: 1
file_date_updated: 2024-01-30T14:15:16Z
has_accepted_license: '1'
intvolume: '       285'
isi: 1
issue: '10'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
publication: Journal of Functional Analysis
publication_identifier:
  eissn:
  - 1096-0783
  issn:
  - 0022-1236
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: A simple approach to Lieb-Thirring type inequalities
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 285
year: '2023'
...
---
_id: '14255'
abstract:
- lang: eng
  text: Toscana virus is a major cause of arboviral disease in humans in the Mediterranean
    basin during summer. However, early virus-host cell interactions and entry mechanisms
    remain poorly characterized. Investigating iPSC-derived human neurons and cell
    lines, we found that virus binding to the cell surface was specific, and 50% of
    bound virions were endocytosed within 10 min. Virions entered Rab5a+ early endosomes
    and, subsequently, Rab7a+ and LAMP-1+ late endosomal compartments. Penetration
    required intact late endosomes and occurred within 30 min following internalization.
    Virus entry relied on vacuolar acidification, with an optimal pH for viral membrane
    fusion at pH 5.5. The pH threshold increased to 5.8 with longer pre-exposure of
    virions to the slightly acidic pH in early endosomes. Strikingly, the particles
    remained infectious after entering late endosomes with a pH below the fusion threshold.
    Overall, our study establishes Toscana virus as a late-penetrating virus and reveals
    an atypical use of vacuolar acidity by this virus to enter host cells.
acknowledged_ssus:
- _id: EM-Fac
acknowledgement: "We acknowledge Elodie Chatre and the Imaging Platform Platim, SFR
  Biosciences, Lyon, as well as Vibor Laketa and the Infectious Diseases Imaging Platform
  (IDIP) at the Center for Integrative Infectious Disease Research (CIID) Heidelberg.
  The sand fly cell lines were supplied by the Tick Cell Biobank at the University
  of Liverpool. F.K.M.S. acknowledges support from the Scientific Service Units (SSUs)
  of ISTA through resources provided by the Electron Microscopy Facility (EMF).\r\nThis
  work was supported by CellNetworks Research Group funds and Deutsche Forschungsgemeinschaft
  (DFG) funding (LO-2338/3-1) and the Agence Nationale de la Recherche (ANR) funding
  (grant numbers ANR-21-CE11-0012 and ANR-22-CE15-0034), all awarded to P.-Y.L. This
  work was also supported by the LABEX ECOFECT (ANR-11-LABX-0048) of Université de
  Lyon (UDL), within the program “Investissements d’Avenir” (ANR-11-IDEX-0007) operated
  by the ANR and by the RESPOND program of the UDL (awarded to P.-Y.L) . C.A. was
  supported by the Chica and Heinz Schaller Research Group funds, NARSAD 2019 award,
  a Fritz Thyssen Research Grant, and the SFB1158-S02 grant. L.B-S. is supported by
  a United Kingdom Biotechnology and Biological Sciences Research Council grant (BB/P024270/1)
  and a Wellcome Trust grant (223743/Z/21/Z). F.K.M.S acknowledges support from the
  Austrian Science Fund (FWF, P31445). J.K. received a salary from the DFG (LO-2338/3-1)
  and then from the ANR (ANR-11-LABX-0048). The salary of Z.M.U. was partially covered
  by the DFG (LO-2338/3-1). S.K. received a salary from the DFG (SFB1129). We are
  grateful to the Chinese Scholarship Council (CSC; 201904910701), DAAD/ANID (57451854/62180003),
  the Rufus A. Kellogg fellowship program (Amherst College, Massachusetts, USA) for
  awarding fellowships to Q.X., J.C., and H.A.A., respectively."
article_number: e1011562
article_processing_charge: Yes
article_type: original
author:
- first_name: Jana
  full_name: Koch, Jana
  last_name: Koch
- first_name: Qilin
  full_name: Xin, Qilin
  last_name: Xin
- first_name: Martin
  full_name: Obr, Martin
  id: 4741CA5A-F248-11E8-B48F-1D18A9856A87
  last_name: Obr
  orcid: 0000-0003-1756-6564
- first_name: Alicia
  full_name: Schäfer, Alicia
  last_name: Schäfer
- first_name: Nina
  full_name: Rolfs, Nina
  last_name: Rolfs
- first_name: Holda A.
  full_name: Anagho, Holda A.
  last_name: Anagho
- first_name: Aiste
  full_name: Kudulyte, Aiste
  last_name: Kudulyte
- first_name: Lea
  full_name: Woltereck, Lea
  last_name: Woltereck
- first_name: Susann
  full_name: Kummer, Susann
  last_name: Kummer
- first_name: Joaquin
  full_name: Campos, Joaquin
  last_name: Campos
- first_name: Zina M.
  full_name: Uckeley, Zina M.
  last_name: Uckeley
- first_name: Lesley
  full_name: Bell-Sakyi, Lesley
  last_name: Bell-Sakyi
- first_name: Hans Georg
  full_name: Kräusslich, Hans Georg
  last_name: Kräusslich
- first_name: Florian Km
  full_name: Schur, Florian Km
  id: 48AD8942-F248-11E8-B48F-1D18A9856A87
  last_name: Schur
  orcid: 0000-0003-4790-8078
- first_name: Claudio
  full_name: Acuna, Claudio
  last_name: Acuna
- first_name: Pierre Yves
  full_name: Lozach, Pierre Yves
  last_name: Lozach
citation:
  ama: Koch J, Xin Q, Obr M, et al. The phenuivirus Toscana virus makes an atypical
    use of vacuolar acidity to enter host cells. <i>PLoS Pathogens</i>. 2023;19(8).
    doi:<a href="https://doi.org/10.1371/journal.ppat.1011562">10.1371/journal.ppat.1011562</a>
  apa: Koch, J., Xin, Q., Obr, M., Schäfer, A., Rolfs, N., Anagho, H. A., … Lozach,
    P. Y. (2023). The phenuivirus Toscana virus makes an atypical use of vacuolar
    acidity to enter host cells. <i>PLoS Pathogens</i>. Public Library of Science.
    <a href="https://doi.org/10.1371/journal.ppat.1011562">https://doi.org/10.1371/journal.ppat.1011562</a>
  chicago: Koch, Jana, Qilin Xin, Martin Obr, Alicia Schäfer, Nina Rolfs, Holda A.
    Anagho, Aiste Kudulyte, et al. “The Phenuivirus Toscana Virus Makes an Atypical
    Use of Vacuolar Acidity to Enter Host Cells.” <i>PLoS Pathogens</i>. Public Library
    of Science, 2023. <a href="https://doi.org/10.1371/journal.ppat.1011562">https://doi.org/10.1371/journal.ppat.1011562</a>.
  ieee: J. Koch <i>et al.</i>, “The phenuivirus Toscana virus makes an atypical use
    of vacuolar acidity to enter host cells,” <i>PLoS Pathogens</i>, vol. 19, no.
    8. Public Library of Science, 2023.
  ista: Koch J, Xin Q, Obr M, Schäfer A, Rolfs N, Anagho HA, Kudulyte A, Woltereck
    L, Kummer S, Campos J, Uckeley ZM, Bell-Sakyi L, Kräusslich HG, Schur FK, Acuna
    C, Lozach PY. 2023. The phenuivirus Toscana virus makes an atypical use of vacuolar
    acidity to enter host cells. PLoS Pathogens. 19(8), e1011562.
  mla: Koch, Jana, et al. “The Phenuivirus Toscana Virus Makes an Atypical Use of
    Vacuolar Acidity to Enter Host Cells.” <i>PLoS Pathogens</i>, vol. 19, no. 8,
    e1011562, Public Library of Science, 2023, doi:<a href="https://doi.org/10.1371/journal.ppat.1011562">10.1371/journal.ppat.1011562</a>.
  short: J. Koch, Q. Xin, M. Obr, A. Schäfer, N. Rolfs, H.A. Anagho, A. Kudulyte,
    L. Woltereck, S. Kummer, J. Campos, Z.M. Uckeley, L. Bell-Sakyi, H.G. Kräusslich,
    F.K. Schur, C. Acuna, P.Y. Lozach, PLoS Pathogens 19 (2023).
date_created: 2023-09-03T22:01:14Z
date_published: 2023-08-14T00:00:00Z
date_updated: 2025-04-15T08:24:50Z
day: '14'
ddc:
- '570'
department:
- _id: FlSc
doi: 10.1371/journal.ppat.1011562
external_id:
  isi:
  - '001050846300004'
  pmid:
  - '37578957'
file:
- access_level: open_access
  checksum: 47ca3bb54b27f28b05644be0ad064bc6
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T06:41:52Z
  date_updated: 2023-09-06T06:41:52Z
  file_id: '14269'
  file_name: 2023_PloSPathogens_Koch.pdf
  file_size: 4458336
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T06:41:52Z
has_accepted_license: '1'
intvolume: '        19'
isi: 1
issue: '8'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 26736D6A-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P31445
  name: Structural conservation and diversity in retroviral capsid
publication: PLoS Pathogens
publication_identifier:
  eissn:
  - 1553-7374
  issn:
  - 1553-7366
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: The phenuivirus Toscana virus makes an atypical use of vacuolar acidity to
  enter host cells
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 19
year: '2023'
...
---
_id: '14256'
abstract:
- lang: eng
  text: "Context. Space asteroseismology is revolutionizing our knowledge of the internal
    structure and dynamics of stars. A breakthrough is ongoing with the recent discoveries
    of signatures of strong magnetic fields in the core of red giant stars. The key
    signature for such a detection is the asymmetry these fields induce in the frequency
    splittings of observed dipolar mixed gravito-acoustic modes.\r\nAims. We investigate
    the ability of the observed asymmetries of the frequency splittings of dipolar
    mixed modes to constrain the geometrical properties of deep magnetic fields.\r\nMethods.
    We used the powerful analytical Racah-Wigner algebra used in quantum mechanics
    to characterize the geometrical couplings of dipolar mixed oscillation modes with
    various realistically plausible topologies of fossil magnetic fields. We also
    computed the induced perturbation of their frequencies.\r\nResults. First, in
    the case of an oblique magnetic dipole, we provide the exact analytical expression
    of the asymmetry as a function of the angle between the rotation and magnetic
    axes. Its value provides a direct measure of this angle. Second, considering a
    combination of axisymmetric dipolar and quadrupolar fields, we show how the asymmetry
    is blind to the unraveling of the relative strength and sign of each component.
    Finally, in the case of a given multipole, we show that a negative asymmetry is
    a signature of non-axisymmetric topologies.\r\nConclusions. Asymmetries of dipolar
    mixed modes provide a key bit of information on the geometrical topology of deep
    fossil magnetic fields, but this is insufficient on its own. Asteroseismic constraints
    should therefore be combined with spectropolarimetric observations and numerical
    simulations, which aim to predict the more probable stable large-scale geometries."
acknowledgement: The authors are grateful to the referee for her/his detailed and
  constructive report, which has allowed us to improve our article. S. M. acknowledges
  support from the CNES GOLF-SOHO and PLATO grants at CEA/DAp and PNPS (CNRS/INSU).
  We thank R. A. Garcia for fruitful discussions and suggestions.
article_number: L9
article_processing_charge: Yes (in subscription journal)
article_type: letter_note
arxiv: 1
author:
- first_name: S.
  full_name: Mathis, S.
  last_name: Mathis
- first_name: Lisa Annabelle
  full_name: Bugnet, Lisa Annabelle
  id: d9edb345-f866-11ec-9b37-d119b5234501
  last_name: Bugnet
  orcid: 0000-0003-0142-4000
citation:
  ama: 'Mathis S, Bugnet LA. Asymmetries of frequency splittings of dipolar mixed
    modes: A window on the topology of deep magnetic fields. <i>Astronomy and Astrophysics</i>.
    2023;676. doi:<a href="https://doi.org/10.1051/0004-6361/202346832">10.1051/0004-6361/202346832</a>'
  apa: 'Mathis, S., &#38; Bugnet, L. A. (2023). Asymmetries of frequency splittings
    of dipolar mixed modes: A window on the topology of deep magnetic fields. <i>Astronomy
    and Astrophysics</i>. EDP Sciences. <a href="https://doi.org/10.1051/0004-6361/202346832">https://doi.org/10.1051/0004-6361/202346832</a>'
  chicago: 'Mathis, S., and Lisa Annabelle Bugnet. “Asymmetries of Frequency Splittings
    of Dipolar Mixed Modes: A Window on the Topology of Deep Magnetic Fields.” <i>Astronomy
    and Astrophysics</i>. EDP Sciences, 2023. <a href="https://doi.org/10.1051/0004-6361/202346832">https://doi.org/10.1051/0004-6361/202346832</a>.'
  ieee: 'S. Mathis and L. A. Bugnet, “Asymmetries of frequency splittings of dipolar
    mixed modes: A window on the topology of deep magnetic fields,” <i>Astronomy and
    Astrophysics</i>, vol. 676. EDP Sciences, 2023.'
  ista: 'Mathis S, Bugnet LA. 2023. Asymmetries of frequency splittings of dipolar
    mixed modes: A window on the topology of deep magnetic fields. Astronomy and Astrophysics.
    676, L9.'
  mla: 'Mathis, S., and Lisa Annabelle Bugnet. “Asymmetries of Frequency Splittings
    of Dipolar Mixed Modes: A Window on the Topology of Deep Magnetic Fields.” <i>Astronomy
    and Astrophysics</i>, vol. 676, L9, EDP Sciences, 2023, doi:<a href="https://doi.org/10.1051/0004-6361/202346832">10.1051/0004-6361/202346832</a>.'
  short: S. Mathis, L.A. Bugnet, Astronomy and Astrophysics 676 (2023).
date_created: 2023-09-03T22:01:15Z
date_published: 2023-08-01T00:00:00Z
date_updated: 2023-09-06T11:05:58Z
day: '01'
ddc:
- '520'
department:
- _id: LiBu
doi: 10.1051/0004-6361/202346832
external_id:
  arxiv:
  - '2306.11587'
  isi:
  - '001046037700007'
file:
- access_level: open_access
  checksum: 7b30d26fb2b7bcb5b5be1414950615f9
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T07:13:19Z
  date_updated: 2023-09-06T07:13:19Z
  file_id: '14271'
  file_name: 2023_AstronomyAstrophysics_Mathis.pdf
  file_size: 458120
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T07:13:19Z
has_accepted_license: '1'
intvolume: '       676'
isi: 1
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
publication: Astronomy and Astrophysics
publication_identifier:
  eissn:
  - 1432-0746
  issn:
  - 0004-6361
publication_status: published
publisher: EDP Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Asymmetries of frequency splittings of dipolar mixed modes: A window on the
  topology of deep magnetic fields'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 676
year: '2023'
...
---
_id: '14258'
abstract:
- lang: eng
  text: There is currently little evidence that the genetic basis of human phenotype
    varies significantly across the lifespan. However, time-to-event phenotypes are
    understudied and can be thought of as reflecting an underlying hazard, which is
    unlikely to be constant through life when values take a broad range. Here, we
    find that 74% of 245 genome-wide significant genetic associations with age at
    natural menopause (ANM) in the UK Biobank show a form of age-specific effect.
    Nineteen of these replicated discoveries are identified only by our modeling framework,
    which determines the time dependency of DNA-variant age-at-onset associations
    without a significant multiple-testing burden. Across the range of early to late
    menopause, we find evidence for significantly different underlying biological
    pathways, changes in the signs of genetic correlations of ANM to health indicators
    and outcomes, and differences in inferred causal relationships. We find that DNA
    damage response processes only act to shape ovarian reserve and depletion for
    women of early ANM. Genetically mediated delays in ANM were associated with increased
    relative risk of breast cancer and leiomyoma at all ages and with high cholesterol
    and heart failure for late-ANM women. These findings suggest that a better understanding
    of the age dependency of genetic risk factor relationships among health indicators
    and outcomes is achievable through appropriate statistical modeling of large-scale
    biobank data.
acknowledgement: This project was funded by an SNSF Eccellenza grant to M.R.R. (PCEGP3-181181)
  and by core funding from the Institute of Science and Technology Austria. K.L. and
  R.M. were supported by the Estonian Research Council grant 1911. Estonian Biobank
  computations were performed in the High-Performance Computing Center, University
  of Tartu. We thank Triin Laisk for her valuable insights and comments that helped
  greatly. We would like to acknowledge the participants and investigators of UK Biobank
  and Estonian Biobank studies. This project uses UK Biobank data under project number
  35520.
article_processing_charge: Yes (via OA deal)
article_type: original
author:
- first_name: Sven E.
  full_name: Ojavee, Sven E.
  last_name: Ojavee
- first_name: Liza
  full_name: Darrous, Liza
  last_name: Darrous
- first_name: Marion
  full_name: Patxot, Marion
  last_name: Patxot
- first_name: Kristi
  full_name: Läll, Kristi
  last_name: Läll
- first_name: Krista
  full_name: Fischer, Krista
  last_name: Fischer
- first_name: Reedik
  full_name: Mägi, Reedik
  last_name: Mägi
- first_name: Zoltan
  full_name: Kutalik, Zoltan
  last_name: Kutalik
- first_name: Matthew Richard
  full_name: Robinson, Matthew Richard
  id: E5D42276-F5DA-11E9-8E24-6303E6697425
  last_name: Robinson
  orcid: 0000-0001-8982-8813
citation:
  ama: Ojavee SE, Darrous L, Patxot M, et al. Genetic insights into the age-specific
    biological mechanisms governing human ovarian aging. <i>American Journal of Human
    Genetics</i>. 2023;110(9):1549-1563. doi:<a href="https://doi.org/10.1016/j.ajhg.2023.07.006">10.1016/j.ajhg.2023.07.006</a>
  apa: Ojavee, S. E., Darrous, L., Patxot, M., Läll, K., Fischer, K., Mägi, R., …
    Robinson, M. R. (2023). Genetic insights into the age-specific biological mechanisms
    governing human ovarian aging. <i>American Journal of Human Genetics</i>. Elsevier.
    <a href="https://doi.org/10.1016/j.ajhg.2023.07.006">https://doi.org/10.1016/j.ajhg.2023.07.006</a>
  chicago: Ojavee, Sven E., Liza Darrous, Marion Patxot, Kristi Läll, Krista Fischer,
    Reedik Mägi, Zoltan Kutalik, and Matthew Richard Robinson. “Genetic Insights into
    the Age-Specific Biological Mechanisms Governing Human Ovarian Aging.” <i>American
    Journal of Human Genetics</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.ajhg.2023.07.006">https://doi.org/10.1016/j.ajhg.2023.07.006</a>.
  ieee: S. E. Ojavee <i>et al.</i>, “Genetic insights into the age-specific biological
    mechanisms governing human ovarian aging,” <i>American Journal of Human Genetics</i>,
    vol. 110, no. 9. Elsevier, pp. 1549–1563, 2023.
  ista: Ojavee SE, Darrous L, Patxot M, Läll K, Fischer K, Mägi R, Kutalik Z, Robinson
    MR. 2023. Genetic insights into the age-specific biological mechanisms governing
    human ovarian aging. American Journal of Human Genetics. 110(9), 1549–1563.
  mla: Ojavee, Sven E., et al. “Genetic Insights into the Age-Specific Biological
    Mechanisms Governing Human Ovarian Aging.” <i>American Journal of Human Genetics</i>,
    vol. 110, no. 9, Elsevier, 2023, pp. 1549–63, doi:<a href="https://doi.org/10.1016/j.ajhg.2023.07.006">10.1016/j.ajhg.2023.07.006</a>.
  short: S.E. Ojavee, L. Darrous, M. Patxot, K. Läll, K. Fischer, R. Mägi, Z. Kutalik,
    M.R. Robinson, American Journal of Human Genetics 110 (2023) 1549–1563.
corr_author: '1'
date_created: 2023-09-03T22:01:15Z
date_published: 2023-09-07T00:00:00Z
date_updated: 2025-09-09T12:51:20Z
day: '07'
ddc:
- '570'
department:
- _id: MaRo
doi: 10.1016/j.ajhg.2023.07.006
external_id:
  isi:
  - '001074842500001'
  pmid:
  - '37543033'
file:
- access_level: open_access
  checksum: 4108b031dc726ae6b4a5ae7e021ba188
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-30T13:20:35Z
  date_updated: 2024-01-30T13:20:35Z
  file_id: '14912'
  file_name: 2023_AJHG_Ojavee.pdf
  file_size: 2551276
  relation: main_file
  success: 1
file_date_updated: 2024-01-30T13:20:35Z
has_accepted_license: '1'
intvolume: '       110'
isi: 1
issue: '9'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: 1549-1563
pmid: 1
publication: American Journal of Human Genetics
publication_identifier:
  eissn:
  - 1537-6605
  issn:
  - 0002-9297
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Genetic insights into the age-specific biological mechanisms governing human
  ovarian aging
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 110
year: '2023'
...
---
_id: '14259'
abstract:
- lang: eng
  text: "We provide a learning-based technique for guessing a winning strategy in
    a parity game originating from an LTL synthesis problem. A cheaply obtained guess
    can be useful in several applications. Not only can the guessed strategy be applied
    as best-effort in cases where the game’s huge size prohibits rigorous approaches,
    but it can also increase the scalability of rigorous LTL synthesis in several
    ways. Firstly, checking whether a guessed strategy is winning is easier than constructing
    one. Secondly, even if the guess is wrong in some places, it can be fixed by strategy
    iteration faster than constructing one from scratch. Thirdly, the guess can be
    used in on-the-fly approaches to prioritize exploration in the most fruitful directions.\r\nIn
    contrast to previous works, we (i) reflect the highly structured logical information
    in game’s states, the so-called semantic labelling, coming from the recent LTL-to-automata
    translations, and (ii) learn to reflect it properly by learning from previously
    solved games, bringing the solving process closer to human-like reasoning."
acknowledgement: This research was funded in part by the German Research Foundation
  (DFG) project 427755713 Group-By Objectives in Probabilistic Verification (GOPro).
alternative_title:
- LNCS
article_processing_charge: Yes (in subscription journal)
author:
- first_name: Jan
  full_name: Kretinsky, Jan
  id: 44CEF464-F248-11E8-B48F-1D18A9856A87
  last_name: Kretinsky
  orcid: 0000-0002-8122-2881
- first_name: Tobias
  full_name: Meggendorfer, Tobias
  id: b21b0c15-30a2-11eb-80dc-f13ca25802e1
  last_name: Meggendorfer
  orcid: 0000-0002-1712-2165
- first_name: Maximilian
  full_name: Prokop, Maximilian
  last_name: Prokop
- first_name: Sabine
  full_name: Rieder, Sabine
  last_name: Rieder
citation:
  ama: 'Kretinsky J, Meggendorfer T, Prokop M, Rieder S. Guessing winning policies
    in LTL synthesis by semantic learning. In: <i>35th International Conference on
    Computer Aided Verification </i>. Vol 13964. Springer Nature; 2023:390-414. doi:<a
    href="https://doi.org/10.1007/978-3-031-37706-8_20">10.1007/978-3-031-37706-8_20</a>'
  apa: 'Kretinsky, J., Meggendorfer, T., Prokop, M., &#38; Rieder, S. (2023). Guessing
    winning policies in LTL synthesis by semantic learning. In <i>35th International
    Conference on Computer Aided Verification </i> (Vol. 13964, pp. 390–414). Paris,
    France: Springer Nature. <a href="https://doi.org/10.1007/978-3-031-37706-8_20">https://doi.org/10.1007/978-3-031-37706-8_20</a>'
  chicago: Kretinsky, Jan, Tobias Meggendorfer, Maximilian Prokop, and Sabine Rieder.
    “Guessing Winning Policies in LTL Synthesis by Semantic Learning.” In <i>35th
    International Conference on Computer Aided Verification </i>, 13964:390–414. Springer
    Nature, 2023. <a href="https://doi.org/10.1007/978-3-031-37706-8_20">https://doi.org/10.1007/978-3-031-37706-8_20</a>.
  ieee: J. Kretinsky, T. Meggendorfer, M. Prokop, and S. Rieder, “Guessing winning
    policies in LTL synthesis by semantic learning,” in <i>35th International Conference
    on Computer Aided Verification </i>, Paris, France, 2023, vol. 13964, pp. 390–414.
  ista: 'Kretinsky J, Meggendorfer T, Prokop M, Rieder S. 2023. Guessing winning policies
    in LTL synthesis by semantic learning. 35th International Conference on Computer
    Aided Verification . CAV: Computer Aided Verification, LNCS, vol. 13964, 390–414.'
  mla: Kretinsky, Jan, et al. “Guessing Winning Policies in LTL Synthesis by Semantic
    Learning.” <i>35th International Conference on Computer Aided Verification </i>,
    vol. 13964, Springer Nature, 2023, pp. 390–414, doi:<a href="https://doi.org/10.1007/978-3-031-37706-8_20">10.1007/978-3-031-37706-8_20</a>.
  short: J. Kretinsky, T. Meggendorfer, M. Prokop, S. Rieder, in:, 35th International
    Conference on Computer Aided Verification , Springer Nature, 2023, pp. 390–414.
conference:
  end_date: 2023-07-22
  location: Paris, France
  name: 'CAV: Computer Aided Verification'
  start_date: 2023-07-17
date_created: 2023-09-03T22:01:16Z
date_published: 2023-07-17T00:00:00Z
date_updated: 2025-09-09T12:52:34Z
day: '17'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1007/978-3-031-37706-8_20
external_id:
  isi:
  - '001310786500020'
file:
- access_level: open_access
  checksum: ed66278b61bb869e1baba3d9b9081271
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T08:25:50Z
  date_updated: 2023-09-06T08:25:50Z
  file_id: '14276'
  file_name: 2023_LNCS_CAV_Kretinsky.pdf
  file_size: 428354
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T08:25:50Z
has_accepted_license: '1'
intvolume: '     13964'
isi: 1
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 390-414
publication: '35th International Conference on Computer Aided Verification '
publication_identifier:
  eissn:
  - 1611-3349
  isbn:
  - '9783031377051'
  issn:
  - 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Guessing winning policies in LTL synthesis by semantic learning
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 13964
year: '2023'
...
---
_id: '14260'
abstract:
- lang: eng
  text: "This paper presents Lincheck, a new practical and user-friendly framework
    for testing concurrent algorithms on the Java Virtual Machine (JVM). Lincheck
    provides a simple and declarative way to write concurrent tests: instead of describing
    how to perform the test, users specify what to test by declaring all the operations
    to examine; the framework automatically handles the rest. As a result, tests written
    with Lincheck are concise and easy to understand. The framework automatically
    generates a set of concurrent scenarios, examines them using stress-testing or
    bounded model checking, and verifies that the results of each invocation are correct.
    Notably, if an error is detected via model checking, Lincheck provides an easy-to-follow
    trace to reproduce it, significantly simplifying the bug investigation.\r\n\r\nTo
    the best of our knowledge, Lincheck is the first production-ready tool on the
    JVM that offers such a simple way of writing concurrent tests, without requiring
    special skills or expertise. We successfully integrated Lincheck in the development
    process of several large projects, such as Kotlin Coroutines, and identified new
    bugs in popular concurrency libraries, such as a race in Java’s standard ConcurrentLinkedDeque
    and a liveliness bug in Java’s AbstractQueuedSynchronizer framework, which is
    used in most of the synchronization primitives. We believe that Lincheck can significantly
    improve the quality and productivity of concurrent algorithms research and development
    and become the state-of-the-art tool for checking their correctness."
alternative_title:
- LNCS
article_processing_charge: Yes (in subscription journal)
author:
- first_name: Nikita
  full_name: Koval, Nikita
  id: 2F4DB10C-F248-11E8-B48F-1D18A9856A87
  last_name: Koval
- first_name: Alexander
  full_name: Fedorov, Alexander
  id: 2e711909-896a-11ed-bdf8-eb0f5a2984c6
  last_name: Fedorov
- first_name: Maria
  full_name: Sokolova, Maria
  last_name: Sokolova
- first_name: Dmitry
  full_name: Tsitelov, Dmitry
  last_name: Tsitelov
- first_name: Dan-Adrian
  full_name: Alistarh, Dan-Adrian
  id: 4A899BFC-F248-11E8-B48F-1D18A9856A87
  last_name: Alistarh
  orcid: 0000-0003-3650-940X
citation:
  ama: 'Koval N, Fedorov A, Sokolova M, Tsitelov D, Alistarh D-A. Lincheck: A practical
    framework for testing concurrent data structures on JVM. In: <i>35th International
    Conference on Computer Aided Verification </i>. Vol 13964. Springer Nature; 2023:156-169.
    doi:<a href="https://doi.org/10.1007/978-3-031-37706-8_8">10.1007/978-3-031-37706-8_8</a>'
  apa: 'Koval, N., Fedorov, A., Sokolova, M., Tsitelov, D., &#38; Alistarh, D.-A.
    (2023). Lincheck: A practical framework for testing concurrent data structures
    on JVM. In <i>35th International Conference on Computer Aided Verification </i>
    (Vol. 13964, pp. 156–169). Paris, France: Springer Nature. <a href="https://doi.org/10.1007/978-3-031-37706-8_8">https://doi.org/10.1007/978-3-031-37706-8_8</a>'
  chicago: 'Koval, Nikita, Alexander Fedorov, Maria Sokolova, Dmitry Tsitelov, and
    Dan-Adrian Alistarh. “Lincheck: A Practical Framework for Testing Concurrent Data
    Structures on JVM.” In <i>35th International Conference on Computer Aided Verification
    </i>, 13964:156–69. Springer Nature, 2023. <a href="https://doi.org/10.1007/978-3-031-37706-8_8">https://doi.org/10.1007/978-3-031-37706-8_8</a>.'
  ieee: 'N. Koval, A. Fedorov, M. Sokolova, D. Tsitelov, and D.-A. Alistarh, “Lincheck:
    A practical framework for testing concurrent data structures on JVM,” in <i>35th
    International Conference on Computer Aided Verification </i>, Paris, France, 2023,
    vol. 13964, pp. 156–169.'
  ista: 'Koval N, Fedorov A, Sokolova M, Tsitelov D, Alistarh D-A. 2023. Lincheck:
    A practical framework for testing concurrent data structures on JVM. 35th International
    Conference on Computer Aided Verification . CAV: Computer Aided Verification,
    LNCS, vol. 13964, 156–169.'
  mla: 'Koval, Nikita, et al. “Lincheck: A Practical Framework for Testing Concurrent
    Data Structures on JVM.” <i>35th International Conference on Computer Aided Verification
    </i>, vol. 13964, Springer Nature, 2023, pp. 156–69, doi:<a href="https://doi.org/10.1007/978-3-031-37706-8_8">10.1007/978-3-031-37706-8_8</a>.'
  short: N. Koval, A. Fedorov, M. Sokolova, D. Tsitelov, D.-A. Alistarh, in:, 35th
    International Conference on Computer Aided Verification , Springer Nature, 2023,
    pp. 156–169.
conference:
  end_date: 2023-07-22
  location: Paris, France
  name: 'CAV: Computer Aided Verification'
  start_date: 2023-07-17
date_created: 2023-09-03T22:01:16Z
date_published: 2023-07-17T00:00:00Z
date_updated: 2025-09-09T12:51:52Z
day: '17'
ddc:
- '000'
department:
- _id: DaAl
- _id: GradSch
doi: 10.1007/978-3-031-37706-8_8
external_id:
  isi:
  - '001310786500008'
file:
- access_level: open_access
  checksum: c346016393123a0a2338ad4d976f61bc
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T08:16:25Z
  date_updated: 2023-09-06T08:16:25Z
  file_id: '14275'
  file_name: 2023_LNCS_Koval.pdf
  file_size: 421408
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T08:16:25Z
has_accepted_license: '1'
intvolume: '     13964'
isi: 1
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 156-169
publication: '35th International Conference on Computer Aided Verification '
publication_identifier:
  eissn:
  - 1611-3349
  isbn:
  - '9783031377051'
  issn:
  - 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  record:
  - id: '14995'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: 'Lincheck: A practical framework for testing concurrent data structures on JVM'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 13964
year: '2023'
...
---
_id: '14261'
abstract:
- lang: eng
  text: In this work, a generalized, adapted Numerov implementation capable of determining
    band structures of periodic quantum systems is outlined. Based on the input potential,
    the presented approach numerically solves the Schrödinger equation in position
    space at each momentum space point. Thus, in addition to the band structure, the
    method inherently provides information about the state functions and probability
    densities in position space at each momentum space point considered. The generalized,
    adapted Numerov framework provided reliable estimates for a variety of increasingly
    complex test suites in one, two, and three dimensions. The accuracy of the proposed
    methodology was benchmarked against results obtained for the analytically solvable
    Kronig-Penney model. Furthermore, the presented numerical solver was applied to
    a model potential representing a 2D optical lattice being a challenging application
    relevant, for example, in the field of quantum computing.
acknowledgement: Financial supports for this work via a PhD scholarship for J. Gamper
  issued by the Leopold-Franzens-University of Innsbruck (Vicerector Prof. Dr Ulrike
  Tanzer) are gratefully acknowledged. The computational results presented have been
  achieved (in part) using the HPC infrastructure of the University of Innsbruck.
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Jakob
  full_name: Gamper, Jakob
  last_name: Gamper
- first_name: Florian
  full_name: Kluibenschedl, Florian
  id: 7499e70e-eb2c-11ec-b98b-f925648bc9d9
  last_name: Kluibenschedl
- first_name: Alexander K.H.
  full_name: Weiss, Alexander K.H.
  last_name: Weiss
- first_name: Thomas S.
  full_name: Hofer, Thomas S.
  last_name: Hofer
citation:
  ama: Gamper J, Kluibenschedl F, Weiss AKH, Hofer TS. Accessing position space wave
    functions in band structure calculations of periodic systems - a generalized,
    adapted numerov implementation for one-, two-, and three-dimensional quantum problems.
    <i>Journal of Physical Chemistry Letters</i>. 2023;14(33):7395-7403. doi:<a href="https://doi.org/10.1021/acs.jpclett.3c01707">10.1021/acs.jpclett.3c01707</a>
  apa: Gamper, J., Kluibenschedl, F., Weiss, A. K. H., &#38; Hofer, T. S. (2023).
    Accessing position space wave functions in band structure calculations of periodic
    systems - a generalized, adapted numerov implementation for one-, two-, and three-dimensional
    quantum problems. <i>Journal of Physical Chemistry Letters</i>. American Chemical
    Society. <a href="https://doi.org/10.1021/acs.jpclett.3c01707">https://doi.org/10.1021/acs.jpclett.3c01707</a>
  chicago: Gamper, Jakob, Florian Kluibenschedl, Alexander K.H. Weiss, and Thomas
    S. Hofer. “Accessing Position Space Wave Functions in Band Structure Calculations
    of Periodic Systems - a Generalized, Adapted Numerov Implementation for One-,
    Two-, and Three-Dimensional Quantum Problems.” <i>Journal of Physical Chemistry
    Letters</i>. American Chemical Society, 2023. <a href="https://doi.org/10.1021/acs.jpclett.3c01707">https://doi.org/10.1021/acs.jpclett.3c01707</a>.
  ieee: J. Gamper, F. Kluibenschedl, A. K. H. Weiss, and T. S. Hofer, “Accessing position
    space wave functions in band structure calculations of periodic systems - a generalized,
    adapted numerov implementation for one-, two-, and three-dimensional quantum problems,”
    <i>Journal of Physical Chemistry Letters</i>, vol. 14, no. 33. American Chemical
    Society, pp. 7395–7403, 2023.
  ista: Gamper J, Kluibenschedl F, Weiss AKH, Hofer TS. 2023. Accessing position space
    wave functions in band structure calculations of periodic systems - a generalized,
    adapted numerov implementation for one-, two-, and three-dimensional quantum problems.
    Journal of Physical Chemistry Letters. 14(33), 7395–7403.
  mla: Gamper, Jakob, et al. “Accessing Position Space Wave Functions in Band Structure
    Calculations of Periodic Systems - a Generalized, Adapted Numerov Implementation
    for One-, Two-, and Three-Dimensional Quantum Problems.” <i>Journal of Physical
    Chemistry Letters</i>, vol. 14, no. 33, American Chemical Society, 2023, pp. 7395–403,
    doi:<a href="https://doi.org/10.1021/acs.jpclett.3c01707">10.1021/acs.jpclett.3c01707</a>.
  short: J. Gamper, F. Kluibenschedl, A.K.H. Weiss, T.S. Hofer, Journal of Physical
    Chemistry Letters 14 (2023) 7395–7403.
date_created: 2023-09-03T22:01:16Z
date_published: 2023-08-11T00:00:00Z
date_updated: 2023-09-06T11:04:31Z
day: '11'
ddc:
- '530'
- '540'
department:
- _id: GradSch
doi: 10.1021/acs.jpclett.3c01707
external_id:
  isi:
  - '001048165800001'
  pmid:
  - '37566743'
file:
- access_level: open_access
  checksum: 637454e2b3a357498d8d622d241c4bf6
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-06T07:32:39Z
  date_updated: 2023-09-06T07:32:39Z
  file_id: '14272'
  file_name: 2023_JourPhysChemistry_Gamper.pdf
  file_size: 4986859
  relation: main_file
  success: 1
file_date_updated: 2023-09-06T07:32:39Z
has_accepted_license: '1'
intvolume: '        14'
isi: 1
issue: '33'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: 7395-7403
pmid: 1
publication: Journal of Physical Chemistry Letters
publication_identifier:
  eissn:
  - 1948-7185
publication_status: published
publisher: American Chemical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Accessing position space wave functions in band structure calculations of periodic
  systems - a generalized, adapted numerov implementation for one-, two-, and three-dimensional
  quantum problems
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 14
year: '2023'
...
---
_id: '14277'
abstract:
- lang: eng
  text: Living tissues are characterized by an intrinsically mechanochemical interplay
    of active physical forces and complex biochemical signaling pathways. Either feature
    alone can give rise to complex emergent phenomena, for example, mechanically driven
    glassy dynamics and rigidity transitions, or chemically driven reaction-diffusion
    instabilities. An important question is how to quantitatively assess the contribution
    of these different cues to the large-scale dynamics of biological materials. We
    address this in Madin-Darby canine kidney (MDCK) monolayers, considering both
    mechanochemical feedback between extracellular signal-regulated kinase (ERK) signaling
    activity and cellular density as well as a mechanically active tissue rheology
    via a self-propelled vertex model. We show that the relative strength of active
    migration forces to mechanochemical couplings controls a transition from a uniform
    active glass to periodic spatiotemporal waves. We parametrize the model from published
    experimental data sets on MDCK monolayers and use it to make new predictions on
    the correlation functions of cellular dynamics and the dynamics of topological
    defects associated with the oscillatory phase of cells. Interestingly, MDCK monolayers
    are best described by an intermediary parameter region in which both mechanochemical
    couplings and noisy active propulsion have a strong influence on the dynamics.
    Finally, we study how tissue rheology and ERK waves produce feedback on one another
    and uncover a mechanism via which tissue fluidity can be controlled by mechanochemical
    waves at both the local and global levels.
acknowledgement: We thank all members of the Hannezo group for discussions and suggestions,
  as well as Sound Wai Phow for technical assistance. This work received funding from
  the European Research Council under the EU Horizon 2020 research and innovation
  program Grant Agreement No. 851288 (E.H.), JSPS KAKENHI Grant No. 21H05290, and
  the Ministry of Education under the Research Centres of Excellence program through
  the MBI at NUS.
article_number: '013001'
article_processing_charge: Yes
article_type: original
author:
- first_name: Daniel R
  full_name: Boocock, Daniel R
  id: 453AF628-F248-11E8-B48F-1D18A9856A87
  last_name: Boocock
  orcid: 0000-0002-1585-2631
- first_name: Tsuyoshi
  full_name: Hirashima, Tsuyoshi
  last_name: Hirashima
- first_name: Edouard B
  full_name: Hannezo, Edouard B
  id: 3A9DB764-F248-11E8-B48F-1D18A9856A87
  last_name: Hannezo
  orcid: 0000-0001-6005-1561
citation:
  ama: Boocock DR, Hirashima T, Hannezo EB. Interplay between mechanochemical patterning
    and glassy dynamics in cellular monolayers. <i>PRX Life</i>. 2023;1(1). doi:<a
    href="https://doi.org/10.1103/prxlife.1.013001">10.1103/prxlife.1.013001</a>
  apa: Boocock, D. R., Hirashima, T., &#38; Hannezo, E. B. (2023). Interplay between
    mechanochemical patterning and glassy dynamics in cellular monolayers. <i>PRX
    Life</i>. American Physical Society. <a href="https://doi.org/10.1103/prxlife.1.013001">https://doi.org/10.1103/prxlife.1.013001</a>
  chicago: Boocock, Daniel R, Tsuyoshi Hirashima, and Edouard B Hannezo. “Interplay
    between Mechanochemical Patterning and Glassy Dynamics in Cellular Monolayers.”
    <i>PRX Life</i>. American Physical Society, 2023. <a href="https://doi.org/10.1103/prxlife.1.013001">https://doi.org/10.1103/prxlife.1.013001</a>.
  ieee: D. R. Boocock, T. Hirashima, and E. B. Hannezo, “Interplay between mechanochemical
    patterning and glassy dynamics in cellular monolayers,” <i>PRX Life</i>, vol.
    1, no. 1. American Physical Society, 2023.
  ista: Boocock DR, Hirashima T, Hannezo EB. 2023. Interplay between mechanochemical
    patterning and glassy dynamics in cellular monolayers. PRX Life. 1(1), 013001.
  mla: Boocock, Daniel R., et al. “Interplay between Mechanochemical Patterning and
    Glassy Dynamics in Cellular Monolayers.” <i>PRX Life</i>, vol. 1, no. 1, 013001,
    American Physical Society, 2023, doi:<a href="https://doi.org/10.1103/prxlife.1.013001">10.1103/prxlife.1.013001</a>.
  short: D.R. Boocock, T. Hirashima, E.B. Hannezo, PRX Life 1 (2023).
corr_author: '1'
date_created: 2023-09-06T08:30:59Z
date_published: 2023-07-20T00:00:00Z
date_updated: 2025-04-14T07:52:27Z
day: '20'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.1103/prxlife.1.013001
ec_funded: 1
file:
- access_level: open_access
  checksum: f881d98c89eb9f1aa136d7b781511553
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-15T06:30:50Z
  date_updated: 2023-09-15T06:30:50Z
  file_id: '14335'
  file_name: 2023_PRXLife_Boocock.pdf
  file_size: 2559520
  relation: main_file
  success: 1
file_date_updated: 2023-09-15T06:30:50Z
has_accepted_license: '1'
intvolume: '         1'
issue: '1'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: 05943252-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '851288'
  name: Design Principles of Branching Morphogenesis
publication: PRX Life
publication_identifier:
  issn:
  - 2835-8279
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
status: public
title: Interplay between mechanochemical patterning and glassy dynamics in cellular
  monolayers
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 1
year: '2023'
...
---
_id: '14279'
abstract:
- lang: eng
  text: "The zip file includes source data used in the manuscript \"CCR7 acts as both
    a sensor and a sink for CCL19 to coordinate collective leukocyte migration\",
    as well as a representative Jupyter notebook to reproduce the main figures. Please
    see the preprint on bioRxiv and the DOI link there to access the final published
    version. Note the title change between the preprint and the published manuscript.\r\nA
    sample script for particle-based simulations of collective chemotaxis by self-generated
    gradients is also included (see Self-generated_chemotaxis_sample_script.ipynb)
    to generate exemplary cell trajectories. A detailed description of the simulation
    setup is provided in the supplementary information of the manuscipt."
article_processing_charge: No
author:
- first_name: Mehmet C
  full_name: Ucar, Mehmet C
  id: 50B2A802-6007-11E9-A42B-EB23E6697425
  last_name: Ucar
  orcid: 0000-0003-0506-4217
citation:
  ama: Ucar MC. Source data for the manuscript “CCR7 acts as both a sensor and a sink
    for CCL19 to coordinate collective leukocyte migration.” 2023. doi:<a href="https://doi.org/10.5281/ZENODO.8133960">10.5281/ZENODO.8133960</a>
  apa: Ucar, M. C. (2023). Source data for the manuscript “CCR7 acts as both a sensor
    and a sink for CCL19 to coordinate collective leukocyte migration.” Zenodo. <a
    href="https://doi.org/10.5281/ZENODO.8133960">https://doi.org/10.5281/ZENODO.8133960</a>
  chicago: Ucar, Mehmet C. “Source Data for the Manuscript ‘CCR7 Acts as Both a Sensor
    and a Sink for CCL19 to Coordinate Collective Leukocyte Migration.’” Zenodo, 2023.
    <a href="https://doi.org/10.5281/ZENODO.8133960">https://doi.org/10.5281/ZENODO.8133960</a>.
  ieee: M. C. Ucar, “Source data for the manuscript ‘CCR7 acts as both a sensor and
    a sink for CCL19 to coordinate collective leukocyte migration.’” Zenodo, 2023.
  ista: Ucar MC. 2023. Source data for the manuscript ‘CCR7 acts as both a sensor
    and a sink for CCL19 to coordinate collective leukocyte migration’, Zenodo, <a
    href="https://doi.org/10.5281/ZENODO.8133960">10.5281/ZENODO.8133960</a>.
  mla: Ucar, Mehmet C. <i>Source Data for the Manuscript “CCR7 Acts as Both a Sensor
    and a Sink for CCL19 to Coordinate Collective Leukocyte Migration.”</i> Zenodo,
    2023, doi:<a href="https://doi.org/10.5281/ZENODO.8133960">10.5281/ZENODO.8133960</a>.
  short: M.C. Ucar, (2023).
corr_author: '1'
date_created: 2023-09-06T08:39:25Z
date_published: 2023-07-11T00:00:00Z
date_updated: 2025-04-15T06:54:33Z
day: '11'
ddc:
- '570'
department:
- _id: EdHa
doi: 10.5281/ZENODO.8133960
has_accepted_license: '1'
main_file_link:
- open_access: '1'
  url: https://doi.org/10.5281/zenodo.8133960
month: '07'
oa: 1
oa_version: Published Version
publisher: Zenodo
related_material:
  record:
  - id: '14274'
    relation: used_in_publication
    status: public
status: public
title: Source data for the manuscript "CCR7 acts as both a sensor and a sink for CCL19
  to coordinate collective leukocyte migration"
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: research_data_reference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '14294'
abstract:
- lang: eng
  text: Growth factors and cytokines signal by binding to the extracellular domains
    of their receptors and drive association and transphosphorylation of the receptor
    intracellular tyrosine kinase domains, initiating downstream signaling cascades.
    To enable systematic exploration of how receptor valency and geometry affects
    signaling outcomes, we designed cyclic homo-oligomers with up to 8 subunits using
    repeat protein building blocks that can be modularly extended. By incorporating
    a de novo designed fibroblast growth-factor receptor (FGFR) binding module into
    these scaffolds, we generated a series of synthetic signaling ligands that exhibit
    potent valency- and geometry-dependent Ca2+ release and MAPK pathway activation.
    The high specificity of the designed agonists reveal distinct roles for two FGFR
    splice variants in driving endothelial and mesenchymal cell fates during early
    vascular development. The ability to incorporate receptor binding domains and
    repeat extensions in a modular fashion makes our designed scaffolds broadly useful
    for probing and manipulating cellular signaling pathways.
article_processing_charge: No
author:
- first_name: Natasha I
  full_name: Edman, Natasha I
  last_name: Edman
- first_name: Rachel L
  full_name: Redler, Rachel L
  last_name: Redler
- first_name: Ashish
  full_name: Phal, Ashish
  last_name: Phal
- first_name: Thomas
  full_name: Schlichthaerle, Thomas
  last_name: Schlichthaerle
- first_name: Sanjay R
  full_name: Srivatsan, Sanjay R
  last_name: Srivatsan
- first_name: Ali
  full_name: Etemadi, Ali
  last_name: Etemadi
- first_name: Seong
  full_name: An, Seong
  last_name: An
- first_name: Andrew
  full_name: Favor, Andrew
  last_name: Favor
- first_name: Devon
  full_name: Ehnes, Devon
  last_name: Ehnes
- first_name: Zhe
  full_name: Li, Zhe
  last_name: Li
- first_name: Florian M
  full_name: Praetorius, Florian M
  id: dfec9381-4341-11ee-8fd8-faa02bba7d62
  last_name: Praetorius
- first_name: Max
  full_name: Gordon, Max
  last_name: Gordon
- first_name: Wei
  full_name: Yang, Wei
  last_name: Yang
- first_name: Brian
  full_name: Coventry, Brian
  last_name: Coventry
- first_name: Derrick R
  full_name: Hicks, Derrick R
  last_name: Hicks
- first_name: Longxing
  full_name: Cao, Longxing
  last_name: Cao
- first_name: Neville
  full_name: Bethel, Neville
  last_name: Bethel
- first_name: Piper
  full_name: Heine, Piper
  last_name: Heine
- first_name: Analisa N
  full_name: Murray, Analisa N
  last_name: Murray
- first_name: Stacey
  full_name: Gerben, Stacey
  last_name: Gerben
- first_name: Lauren
  full_name: Carter, Lauren
  last_name: Carter
- first_name: Marcos
  full_name: Miranda, Marcos
  last_name: Miranda
- first_name: Babak
  full_name: Negahdari, Babak
  last_name: Negahdari
- first_name: Sangwon
  full_name: Lee, Sangwon
  last_name: Lee
- first_name: Cole
  full_name: Trapnell, Cole
  last_name: Trapnell
- first_name: Lance
  full_name: Stewart, Lance
  last_name: Stewart
- first_name: Damian C
  full_name: Ekiert, Damian C
  last_name: Ekiert
- first_name: Joseph
  full_name: Schlessinger, Joseph
  last_name: Schlessinger
- first_name: Jay
  full_name: Shendure, Jay
  last_name: Shendure
- first_name: Gira
  full_name: Bhabha, Gira
  last_name: Bhabha
- first_name: Hannele
  full_name: Ruohola-Baker, Hannele
  last_name: Ruohola-Baker
- first_name: David
  full_name: Baker, David
  last_name: Baker
citation:
  ama: Edman NI, Redler RL, Phal A, et al. Modulation of FGF pathway signaling and
    vascular differentiation using designed oligomeric assemblies. <i>bioRxiv</i>.
    doi:<a href="https://doi.org/10.1101/2023.03.14.532666">10.1101/2023.03.14.532666</a>
  apa: Edman, N. I., Redler, R. L., Phal, A., Schlichthaerle, T., Srivatsan, S. R.,
    Etemadi, A., … Baker, D. (n.d.). Modulation of FGF pathway signaling and vascular
    differentiation using designed oligomeric assemblies. <i>bioRxiv</i>. <a href="https://doi.org/10.1101/2023.03.14.532666">https://doi.org/10.1101/2023.03.14.532666</a>
  chicago: Edman, Natasha I, Rachel L Redler, Ashish Phal, Thomas Schlichthaerle,
    Sanjay R Srivatsan, Ali Etemadi, Seong An, et al. “Modulation of FGF Pathway Signaling
    and Vascular Differentiation Using Designed Oligomeric Assemblies.” <i>BioRxiv</i>,
    n.d. <a href="https://doi.org/10.1101/2023.03.14.532666">https://doi.org/10.1101/2023.03.14.532666</a>.
  ieee: N. I. Edman <i>et al.</i>, “Modulation of FGF pathway signaling and vascular
    differentiation using designed oligomeric assemblies,” <i>bioRxiv</i>. .
  ista: Edman NI, Redler RL, Phal A, Schlichthaerle T, Srivatsan SR, Etemadi A, An
    S, Favor A, Ehnes D, Li Z, Praetorius FM, Gordon M, Yang W, Coventry B, Hicks
    DR, Cao L, Bethel N, Heine P, Murray AN, Gerben S, Carter L, Miranda M, Negahdari
    B, Lee S, Trapnell C, Stewart L, Ekiert DC, Schlessinger J, Shendure J, Bhabha
    G, Ruohola-Baker H, Baker D. Modulation of FGF pathway signaling and vascular
    differentiation using designed oligomeric assemblies. bioRxiv, <a href="https://doi.org/10.1101/2023.03.14.532666">10.1101/2023.03.14.532666</a>.
  mla: Edman, Natasha I., et al. “Modulation of FGF Pathway Signaling and Vascular
    Differentiation Using Designed Oligomeric Assemblies.” <i>BioRxiv</i>, doi:<a
    href="https://doi.org/10.1101/2023.03.14.532666">10.1101/2023.03.14.532666</a>.
  short: N.I. Edman, R.L. Redler, A. Phal, T. Schlichthaerle, S.R. Srivatsan, A. Etemadi,
    S. An, A. Favor, D. Ehnes, Z. Li, F.M. Praetorius, M. Gordon, W. Yang, B. Coventry,
    D.R. Hicks, L. Cao, N. Bethel, P. Heine, A.N. Murray, S. Gerben, L. Carter, M.
    Miranda, B. Negahdari, S. Lee, C. Trapnell, L. Stewart, D.C. Ekiert, J. Schlessinger,
    J. Shendure, G. Bhabha, H. Ruohola-Baker, D. Baker, BioRxiv (n.d.).
date_created: 2023-09-06T12:31:49Z
date_published: 2023-03-15T00:00:00Z
date_updated: 2023-11-07T12:21:58Z
day: '15'
doi: 10.1101/2023.03.14.532666
extern: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1101/2023.03.14.532666
month: '03'
oa: 1
oa_version: Preprint
publication: bioRxiv
publication_status: submitted
status: public
title: Modulation of FGF pathway signaling and vascular differentiation using designed
  oligomeric assemblies
type: preprint
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2023'
...
---
_id: '14313'
abstract:
- lang: eng
  text: To respond to auxin, the chief orchestrator of their multicellularity, plants
    evolved multiple receptor systems and signal transduction cascades. Despite decades
    of research, however, we are still lacking a satisfactory synthesis of various
    auxin signaling mechanisms. The chief discrepancy and historical controversy of
    the field is that of rapid and slow auxin effects on plant physiology and development.
    How is it possible that ions begin to trickle across the plasma membrane as soon
    as auxin enters the cell, even though the best-characterized transcriptional auxin
    pathway can take effect only after tens of minutes? Recently, unexpected progress
    has been made in understanding this and other unknowns of auxin signaling. We
    provide a perspective on these exciting developments and concepts whose general
    applicability might have ramifications beyond auxin signaling.
acknowledgement: The opening quote is not intended to reflect any political views
  of the authors. The authors by no means endorse the rhetoric of Donald Rumsfeld
  or the 2003 invasion of Iraq by the United States. Nevertheless, Rumsfeld's quote
  led to both public and academic debates on the concept of known and unknown unknowns,
  which can be applied to the recent unexpected developments in the auxin signaling
  field. We thank Linlin Qi and Huihuang Chen for their suggestions on figure presentation
  and inspiring discussions of TIR1/AFB signaling. Finally, we thank Aroosa Hussain
  for discussion of Greek mythology.
article_number: '102443'
article_processing_charge: No
article_type: review
author:
- first_name: Lukas
  full_name: Fiedler, Lukas
  id: 7c417475-8972-11ed-ae7b-8b674ca26986
  last_name: Fiedler
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
citation:
  ama: 'Fiedler L, Friml J. Rapid auxin signaling: Unknowns old and new. <i>Current
    Opinion in Plant Biology</i>. 2023;75(10). doi:<a href="https://doi.org/10.1016/j.pbi.2023.102443">10.1016/j.pbi.2023.102443</a>'
  apa: 'Fiedler, L., &#38; Friml, J. (2023). Rapid auxin signaling: Unknowns old and
    new. <i>Current Opinion in Plant Biology</i>. Elsevier. <a href="https://doi.org/10.1016/j.pbi.2023.102443">https://doi.org/10.1016/j.pbi.2023.102443</a>'
  chicago: 'Fiedler, Lukas, and Jiří Friml. “Rapid Auxin Signaling: Unknowns Old and
    New.” <i>Current Opinion in Plant Biology</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.pbi.2023.102443">https://doi.org/10.1016/j.pbi.2023.102443</a>.'
  ieee: 'L. Fiedler and J. Friml, “Rapid auxin signaling: Unknowns old and new,” <i>Current
    Opinion in Plant Biology</i>, vol. 75, no. 10. Elsevier, 2023.'
  ista: 'Fiedler L, Friml J. 2023. Rapid auxin signaling: Unknowns old and new. Current
    Opinion in Plant Biology. 75(10), 102443.'
  mla: 'Fiedler, Lukas, and Jiří Friml. “Rapid Auxin Signaling: Unknowns Old and New.”
    <i>Current Opinion in Plant Biology</i>, vol. 75, no. 10, 102443, Elsevier, 2023,
    doi:<a href="https://doi.org/10.1016/j.pbi.2023.102443">10.1016/j.pbi.2023.102443</a>.'
  short: L. Fiedler, J. Friml, Current Opinion in Plant Biology 75 (2023).
corr_author: '1'
date_created: 2023-09-10T22:01:11Z
date_published: 2023-10-01T00:00:00Z
date_updated: 2025-09-09T12:54:16Z
day: '01'
ddc:
- '580'
department:
- _id: JiFr
doi: 10.1016/j.pbi.2023.102443
external_id:
  isi:
  - '001080095300001'
  pmid:
  - '37666097'
file:
- access_level: open_access
  checksum: 1c476c3414d2dfb0c85db0cb6cfd8a28
  content_type: application/pdf
  creator: amally
  date_created: 2023-11-02T17:03:20Z
  date_updated: 2023-11-02T17:03:20Z
  file_id: '14482'
  file_name: Fiedler CurrOpinOlantBiol 2023_revised.pdf
  file_size: 737872
  relation: main_file
  success: 1
file_date_updated: 2023-11-02T17:03:20Z
has_accepted_license: '1'
intvolume: '        75'
isi: 1
issue: '10'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Submitted Version
pmid: 1
publication: Current Opinion in Plant Biology
publication_identifier:
  issn:
  - 1369-5266
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Rapid auxin signaling: Unknowns old and new'
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 75
year: '2023'
...
---
_id: '14314'
abstract:
- lang: eng
  text: The execution of cognitive functions requires coordinated circuit activity
    across different brain areas that involves the associated firing of neuronal assemblies.
    Here, we tested the circuit mechanism behind assembly interactions between the
    hippocampus and the medial prefrontal cortex (mPFC) of adult rats by recording
    neuronal populations during a rule-switching task. We identified functionally
    coupled CA1-mPFC cells that synchronized their activity beyond that expected from
    common spatial coding or oscillatory firing. When such cell pairs fired together,
    the mPFC cell strongly phase locked to CA1 theta oscillations and maintained consistent
    theta firing phases, independent of the theta timing of their CA1 counterpart.
    These functionally connected CA1-mPFC cells formed interconnected assemblies.
    While firing together with their CA1 assembly partners, mPFC cells fired along
    specific theta sequences. Our results suggest that upregulated theta oscillatory
    firing of mPFC cells can signal transient interactions with specific CA1 assemblies,
    thus enabling distributed computations.
acknowledgement: We thank A. Cumpelik, H. Chiossi, and L. Bollman for comments on
  an earlier version of this manuscript. This work was funded by EU-FP7 MC-ITN IN-SENS
  (grant 607616).
article_number: '113015'
article_processing_charge: Yes
article_type: original
author:
- first_name: Michele
  full_name: Nardin, Michele
  id: 30BD0376-F248-11E8-B48F-1D18A9856A87
  last_name: Nardin
  orcid: 0000-0001-8849-6570
- first_name: Karola
  full_name: Käfer, Karola
  id: 2DAA49AA-F248-11E8-B48F-1D18A9856A87
  last_name: Käfer
- first_name: Federico
  full_name: Stella, Federico
  id: 39AF1E74-F248-11E8-B48F-1D18A9856A87
  last_name: Stella
  orcid: 0000-0001-9439-3148
- first_name: Jozsef L
  full_name: Csicsvari, Jozsef L
  id: 3FA14672-F248-11E8-B48F-1D18A9856A87
  last_name: Csicsvari
  orcid: 0000-0002-5193-4036
citation:
  ama: Nardin M, Käfer K, Stella F, Csicsvari JL. Theta oscillations as a substrate
    for medial prefrontal-hippocampal assembly interactions. <i>Cell Reports</i>.
    2023;42(9). doi:<a href="https://doi.org/10.1016/j.celrep.2023.113015">10.1016/j.celrep.2023.113015</a>
  apa: Nardin, M., Käfer, K., Stella, F., &#38; Csicsvari, J. L. (2023). Theta oscillations
    as a substrate for medial prefrontal-hippocampal assembly interactions. <i>Cell
    Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2023.113015">https://doi.org/10.1016/j.celrep.2023.113015</a>
  chicago: Nardin, Michele, Karola Käfer, Federico Stella, and Jozsef L Csicsvari.
    “Theta Oscillations as a Substrate for Medial Prefrontal-Hippocampal Assembly
    Interactions.” <i>Cell Reports</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.celrep.2023.113015">https://doi.org/10.1016/j.celrep.2023.113015</a>.
  ieee: M. Nardin, K. Käfer, F. Stella, and J. L. Csicsvari, “Theta oscillations as
    a substrate for medial prefrontal-hippocampal assembly interactions,” <i>Cell
    Reports</i>, vol. 42, no. 9. Elsevier, 2023.
  ista: Nardin M, Käfer K, Stella F, Csicsvari JL. 2023. Theta oscillations as a substrate
    for medial prefrontal-hippocampal assembly interactions. Cell Reports. 42(9),
    113015.
  mla: Nardin, Michele, et al. “Theta Oscillations as a Substrate for Medial Prefrontal-Hippocampal
    Assembly Interactions.” <i>Cell Reports</i>, vol. 42, no. 9, 113015, Elsevier,
    2023, doi:<a href="https://doi.org/10.1016/j.celrep.2023.113015">10.1016/j.celrep.2023.113015</a>.
  short: M. Nardin, K. Käfer, F. Stella, J.L. Csicsvari, Cell Reports 42 (2023).
corr_author: '1'
date_created: 2023-09-10T22:01:11Z
date_published: 2023-09-26T00:00:00Z
date_updated: 2025-09-09T12:53:32Z
day: '26'
ddc:
- '570'
department:
- _id: JoCs
doi: 10.1016/j.celrep.2023.113015
ec_funded: 1
external_id:
  isi:
  - '001068779200001'
  pmid:
  - '37632747'
file:
- access_level: open_access
  checksum: ca77a304fb813c292550b8604b0fb41d
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-15T07:12:46Z
  date_updated: 2023-09-15T07:12:46Z
  file_id: '14337'
  file_name: 2023_CellPress_Nardin.pdf
  file_size: 4879455
  relation: main_file
  success: 1
file_date_updated: 2023-09-15T07:12:46Z
has_accepted_license: '1'
intvolume: '        42'
isi: 1
issue: '9'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 257BBB4C-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '607616'
  name: inter-and intracellular signalling in schizophrenia
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Theta oscillations as a substrate for medial prefrontal-hippocampal assembly
  interactions
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 42
year: '2023'
...
---
_id: '14315'
abstract:
- lang: eng
  text: During apoptosis, caspases degrade 8 out of ~30 nucleoporins to irreversibly
    demolish the nuclear pore complex. However, for poorly understood reasons, caspases
    are also activated during cell differentiation. Here, we show that sublethal activation
    of caspases during myogenesis results in the transient proteolysis of four peripheral
    Nups and one transmembrane Nup. ‘Trimmed’ NPCs become nuclear export-defective,
    and we identified in an unbiased manner several classes of cytoplasmic, plasma
    membrane, and mitochondrial proteins that rapidly accumulate in the nucleus. NPC
    trimming by non-apoptotic caspases was also observed in neurogenesis and endoplasmic
    reticulum stress. Our results suggest that caspases can reversibly modulate nuclear
    transport activity, which allows them to function as agents of cell differentiation
    and adaptation at sublethal levels.
acknowledgement: 'We thank the members of the Hetzer laboratory, Tony Hunter (Salk),
  Lorenzo Puri (Sanford Burnham Prebys), and Jongmin Kim (Massachusetts General Hospital)
  for the critical reading of the manuscript; Kenneth Diffenderfer and Aimee Pankonin
  (Stem Cell Core at the Salk Institute) for help with neurogenesis; Carol Marchetto
  and Fred Gage (Salk) for providing H9 embryonic stem cells; Lorenzo Puri, Alexandra
  Sacco, and Luca Caputo (Sanford Burnham Prebys) for helpful discussions and sharing
  mouse primary myoblasts. This work was supported by a Glenn Foundation for Medical
  Research Postdoctoral Fellowship in Aging Research (UHC), the NOMIS foundation (MWH),
  and the National Institutes of Health (R01 NS096786 to MWH and K01 AR080828 to UHC).
  This work was also supported by the Mass Spectrometry Core of the Salk Institute
  with funding from NIH-NCI CCSG: P30 014195 and the Helmsley Center for Genomic Medicine.
  We thank Jolene Diedrich and Antonio Pinto for technical support.'
article_number: RP89066
article_processing_charge: Yes
article_type: original
author:
- first_name: Ukrae H.
  full_name: Cho, Ukrae H.
  last_name: Cho
- first_name: Martin W
  full_name: Hetzer, Martin W
  id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
  last_name: Hetzer
  orcid: 0000-0002-2111-992X
citation:
  ama: Cho UH, Hetzer M. Caspase-mediated nuclear pore complex trimming in cell differentiation
    and endoplasmic reticulum stress. <i>eLife</i>. 2023;12. doi:<a href="https://doi.org/10.7554/eLife.89066">10.7554/eLife.89066</a>
  apa: Cho, U. H., &#38; Hetzer, M. (2023). Caspase-mediated nuclear pore complex
    trimming in cell differentiation and endoplasmic reticulum stress. <i>ELife</i>.
    eLife Sciences Publications. <a href="https://doi.org/10.7554/eLife.89066">https://doi.org/10.7554/eLife.89066</a>
  chicago: Cho, Ukrae H., and Martin Hetzer. “Caspase-Mediated Nuclear Pore Complex
    Trimming in Cell Differentiation and Endoplasmic Reticulum Stress.” <i>ELife</i>.
    eLife Sciences Publications, 2023. <a href="https://doi.org/10.7554/eLife.89066">https://doi.org/10.7554/eLife.89066</a>.
  ieee: U. H. Cho and M. Hetzer, “Caspase-mediated nuclear pore complex trimming in
    cell differentiation and endoplasmic reticulum stress,” <i>eLife</i>, vol. 12.
    eLife Sciences Publications, 2023.
  ista: Cho UH, Hetzer M. 2023. Caspase-mediated nuclear pore complex trimming in
    cell differentiation and endoplasmic reticulum stress. eLife. 12, RP89066.
  mla: Cho, Ukrae H., and Martin Hetzer. “Caspase-Mediated Nuclear Pore Complex Trimming
    in Cell Differentiation and Endoplasmic Reticulum Stress.” <i>ELife</i>, vol.
    12, RP89066, eLife Sciences Publications, 2023, doi:<a href="https://doi.org/10.7554/eLife.89066">10.7554/eLife.89066</a>.
  short: U.H. Cho, M. Hetzer, ELife 12 (2023).
corr_author: '1'
date_created: 2023-09-10T22:01:11Z
date_published: 2023-09-04T00:00:00Z
date_updated: 2024-10-09T21:06:57Z
day: '04'
ddc:
- '570'
department:
- _id: MaHe
doi: 10.7554/eLife.89066
external_id:
  pmid:
  - '37665327'
file:
- access_level: open_access
  checksum: db24bf3d595507387b48d3799c33e289
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-15T06:59:10Z
  date_updated: 2023-09-15T06:59:10Z
  file_id: '14336'
  file_name: 2023_eLife_Cho.pdf
  file_size: 3703097
  relation: main_file
  success: 1
file_date_updated: 2023-09-15T06:59:10Z
has_accepted_license: '1'
intvolume: '        12'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
publication: eLife
publication_identifier:
  eissn:
  - 2050-084X
publication_status: published
publisher: eLife Sciences Publications
quality_controlled: '1'
scopus_import: '1'
status: public
title: Caspase-mediated nuclear pore complex trimming in cell differentiation and
  endoplasmic reticulum stress
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 12
year: '2023'
...
---
_id: '14316'
abstract:
- lang: eng
  text: Clathrin-mediated vesicle trafficking plays central roles in post-Golgi transport.
    In yeast (Saccharomyces cerevisiae), the AP-1 complex and GGA adaptors are predicted
    to generate distinct transport vesicles at the trans-Golgi network (TGN), and
    the epsin-related proteins Ent3p and Ent5p (collectively Ent3p/5p) act as accessories
    for these adaptors. Recently, we showed that vesicle transport from the TGN is
    crucial for yeast Rab5 (Vps21p)-mediated endosome formation, and that Ent3p/5p
    are crucial for this process, whereas AP-1 and GGA adaptors are dispensable. However,
    these observations were incompatible with previous studies showing that these
    adaptors are required for Ent3p/5p recruitment to the TGN, and thus the overall
    mechanism responsible for regulation of Vps21p activity remains ambiguous. Here,
    we investigated the functional relationships between clathrin adaptors in post-Golgi-mediated
    Vps21p activation. We show that AP-1 disruption in the ent3Δ5Δ mutant impaired
    transport of the Vps21p guanine nucleotide exchange factor Vps9p transport to
    the Vps21p compartment and severely reduced Vps21p activity. Additionally, GGA
    adaptors, the phosphatidylinositol-4-kinase Pik1p and Rab11 GTPases Ypt31p and
    Ypt32p were found to have partially overlapping functions for recruitment of AP-1
    and Ent3p/5p to the TGN. These findings suggest a distinct role of clathrin adaptors
    for Vps21p activation in the TGN–endosome trafficking pathway.
article_number: jcs261448
article_processing_charge: No
article_type: original
author:
- first_name: Makoto
  full_name: Nagano, Makoto
  last_name: Nagano
- first_name: Kaito
  full_name: Aoshima, Kaito
  last_name: Aoshima
- first_name: Hiroki
  full_name: Shimamura, Hiroki
  last_name: Shimamura
- first_name: Daria E
  full_name: Siekhaus, Daria E
  id: 3D224B9E-F248-11E8-B48F-1D18A9856A87
  last_name: Siekhaus
  orcid: 0000-0001-8323-8353
- first_name: Junko Y.
  full_name: Toshima, Junko Y.
  last_name: Toshima
- first_name: Jiro
  full_name: Toshima, Jiro
  last_name: Toshima
citation:
  ama: Nagano M, Aoshima K, Shimamura H, Siekhaus DE, Toshima JY, Toshima J. Distinct
    role of TGN-resident clathrin adaptors for Vps21p activation in the TGN-endosome
    trafficking pathway. <i>Journal of Cell Science</i>. 2023;136(17). doi:<a href="https://doi.org/10.1242/jcs.261448">10.1242/jcs.261448</a>
  apa: Nagano, M., Aoshima, K., Shimamura, H., Siekhaus, D. E., Toshima, J. Y., &#38;
    Toshima, J. (2023). Distinct role of TGN-resident clathrin adaptors for Vps21p
    activation in the TGN-endosome trafficking pathway. <i>Journal of Cell Science</i>.
    The Company of Biologists. <a href="https://doi.org/10.1242/jcs.261448">https://doi.org/10.1242/jcs.261448</a>
  chicago: Nagano, Makoto, Kaito Aoshima, Hiroki Shimamura, Daria E Siekhaus, Junko
    Y. Toshima, and Jiro Toshima. “Distinct Role of TGN-Resident Clathrin Adaptors
    for Vps21p Activation in the TGN-Endosome Trafficking Pathway.” <i>Journal of
    Cell Science</i>. The Company of Biologists, 2023. <a href="https://doi.org/10.1242/jcs.261448">https://doi.org/10.1242/jcs.261448</a>.
  ieee: M. Nagano, K. Aoshima, H. Shimamura, D. E. Siekhaus, J. Y. Toshima, and J.
    Toshima, “Distinct role of TGN-resident clathrin adaptors for Vps21p activation
    in the TGN-endosome trafficking pathway,” <i>Journal of Cell Science</i>, vol.
    136, no. 17. The Company of Biologists, 2023.
  ista: Nagano M, Aoshima K, Shimamura H, Siekhaus DE, Toshima JY, Toshima J. 2023.
    Distinct role of TGN-resident clathrin adaptors for Vps21p activation in the TGN-endosome
    trafficking pathway. Journal of Cell Science. 136(17), jcs261448.
  mla: Nagano, Makoto, et al. “Distinct Role of TGN-Resident Clathrin Adaptors for
    Vps21p Activation in the TGN-Endosome Trafficking Pathway.” <i>Journal of Cell
    Science</i>, vol. 136, no. 17, jcs261448, The Company of Biologists, 2023, doi:<a
    href="https://doi.org/10.1242/jcs.261448">10.1242/jcs.261448</a>.
  short: M. Nagano, K. Aoshima, H. Shimamura, D.E. Siekhaus, J.Y. Toshima, J. Toshima,
    Journal of Cell Science 136 (2023).
date_created: 2023-09-10T22:01:12Z
date_published: 2023-09-01T00:00:00Z
date_updated: 2025-09-09T12:56:46Z
day: '01'
department:
- _id: DaSi
doi: 10.1242/jcs.261448
external_id:
  isi:
  - '001112832300005'
  pmid:
  - '37539494'
intvolume: '       136'
isi: 1
issue: '17'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1101/2023.03.27.534325
month: '09'
oa: 1
oa_version: Preprint
pmid: 1
publication: Journal of Cell Science
publication_identifier:
  eissn:
  - 1477-9137
  issn:
  - 0021-9533
publication_status: published
publisher: The Company of Biologists
quality_controlled: '1'
scopus_import: '1'
status: public
title: Distinct role of TGN-resident clathrin adaptors for Vps21p activation in the
  TGN-endosome trafficking pathway
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 136
year: '2023'
...
---
_id: '14317'
abstract:
- lang: eng
  text: "Markov decision processes can be viewed as transformers of probability distributions.
    While this view is useful from a practical standpoint to reason about trajectories
    of distributions, basic reachability and safety problems are known to be computationally
    intractable (i.e., Skolem-hard) to solve in such models. Further, we show that
    even for simple examples of MDPs, strategies for safety objectives over distributions
    can require infinite memory and randomization.\r\nIn light of this, we present
    a novel overapproximation approach to synthesize strategies in an MDP, such that
    a safety objective over the distributions is met. More precisely, we develop a
    new framework for template-based synthesis of certificates as affine distributional
    and inductive invariants for safety objectives in MDPs. We provide two algorithms
    within this framework. One can only synthesize memoryless strategies, but has
    relative completeness guarantees, while the other can synthesize general strategies.
    The runtime complexity of both algorithms is in PSPACE. We implement these algorithms
    and show that they can solve several non-trivial examples."
acknowledgement: This work was supported in part by the ERC CoG 863818 (FoRM-SMArt)
  and the European Union’s Horizon 2020 research and innovation programme under the
  Marie Skłodowska-Curie Grant Agreement No. 665385 as well as DST/CEFIPRA/INRIA project
  EQuaVE and SERB Matrices grant MTR/2018/00074.
alternative_title:
- LNCS
article_processing_charge: Yes (in subscription journal)
author:
- first_name: S.
  full_name: Akshay, S.
  last_name: Akshay
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Tobias
  full_name: Meggendorfer, Tobias
  id: b21b0c15-30a2-11eb-80dc-f13ca25802e1
  last_name: Meggendorfer
  orcid: 0000-0002-1712-2165
- first_name: Dorde
  full_name: Zikelic, Dorde
  id: 294AA7A6-F248-11E8-B48F-1D18A9856A87
  last_name: Zikelic
  orcid: 0000-0002-4681-1699
citation:
  ama: 'Akshay S, Chatterjee K, Meggendorfer T, Zikelic D. MDPs as distribution transformers:
    Affine invariant synthesis for safety objectives. In: <i>International Conference
    on Computer Aided Verification</i>. Vol 13966. Springer Nature; 2023:86-112. doi:<a
    href="https://doi.org/10.1007/978-3-031-37709-9_5">10.1007/978-3-031-37709-9_5</a>'
  apa: 'Akshay, S., Chatterjee, K., Meggendorfer, T., &#38; Zikelic, D. (2023). MDPs
    as distribution transformers: Affine invariant synthesis for safety objectives.
    In <i>International Conference on Computer Aided Verification</i> (Vol. 13966,
    pp. 86–112). Paris, France: Springer Nature. <a href="https://doi.org/10.1007/978-3-031-37709-9_5">https://doi.org/10.1007/978-3-031-37709-9_5</a>'
  chicago: 'Akshay, S., Krishnendu Chatterjee, Tobias Meggendorfer, and Dorde Zikelic.
    “MDPs as Distribution Transformers: Affine Invariant Synthesis for Safety Objectives.”
    In <i>International Conference on Computer Aided Verification</i>, 13966:86–112.
    Springer Nature, 2023. <a href="https://doi.org/10.1007/978-3-031-37709-9_5">https://doi.org/10.1007/978-3-031-37709-9_5</a>.'
  ieee: 'S. Akshay, K. Chatterjee, T. Meggendorfer, and D. Zikelic, “MDPs as distribution
    transformers: Affine invariant synthesis for safety objectives,” in <i>International
    Conference on Computer Aided Verification</i>, Paris, France, 2023, vol. 13966,
    pp. 86–112.'
  ista: 'Akshay S, Chatterjee K, Meggendorfer T, Zikelic D. 2023. MDPs as distribution
    transformers: Affine invariant synthesis for safety objectives. International
    Conference on Computer Aided Verification. CAV: Computer Aided Verification, LNCS,
    vol. 13966, 86–112.'
  mla: 'Akshay, S., et al. “MDPs as Distribution Transformers: Affine Invariant Synthesis
    for Safety Objectives.” <i>International Conference on Computer Aided Verification</i>,
    vol. 13966, Springer Nature, 2023, pp. 86–112, doi:<a href="https://doi.org/10.1007/978-3-031-37709-9_5">10.1007/978-3-031-37709-9_5</a>.'
  short: S. Akshay, K. Chatterjee, T. Meggendorfer, D. Zikelic, in:, International
    Conference on Computer Aided Verification, Springer Nature, 2023, pp. 86–112.
conference:
  end_date: 2023-07-22
  location: Paris, France
  name: 'CAV: Computer Aided Verification'
  start_date: 2023-07-17
date_created: 2023-09-10T22:01:12Z
date_published: 2023-07-17T00:00:00Z
date_updated: 2025-09-09T12:56:00Z
day: '17'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1007/978-3-031-37709-9_5
ec_funded: 1
external_id:
  isi:
  - '001310805600005'
file:
- access_level: open_access
  checksum: f143c8eedf609f20f2aad2eeb496d53f
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-20T08:46:43Z
  date_updated: 2023-09-20T08:46:43Z
  file_id: '14349'
  file_name: 2023_LNCS_Akshay.pdf
  file_size: 531745
  relation: main_file
  success: 1
file_date_updated: 2023-09-20T08:46:43Z
has_accepted_license: '1'
intvolume: '     13966'
isi: 1
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 86-112
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: 0599E47C-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '863818'
  name: 'Formal Methods for Stochastic Models: Algorithms and Applications'
publication: International Conference on Computer Aided Verification
publication_identifier:
  eissn:
  - 1611-3349
  isbn:
  - '9783031377082'
  issn:
  - 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'MDPs as distribution transformers: Affine invariant synthesis for safety objectives'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 13966
year: '2023'
...
---
_id: '14318'
abstract:
- lang: eng
  text: "Probabilistic recurrence relations (PRRs) are a standard formalism for describing
    the runtime of a randomized algorithm. Given a PRR and a time limit κ, we consider
    the tail probability Pr[T≥κ], i.e., the probability that the randomized runtime
    T of the PRR exceeds κ. Our focus is the formal analysis of tail bounds that aims
    at finding a tight asymptotic upper bound u≥Pr[T≥κ]. To address this problem,
    the classical and most well-known approach is the cookbook method by Karp (JACM
    1994), while other approaches are mostly limited to deriving tail bounds of specific
    PRRs via involved custom analysis.\r\nIn this work, we propose a novel approach
    for deriving the common exponentially-decreasing tail bounds for PRRs whose preprocessing
    time and random passed sizes observe discrete or (piecewise) uniform distribution
    and whose recursive call is either a single procedure call or a divide-and-conquer.
    We first establish a theoretical approach via Markov’s inequality, and then instantiate
    the theoretical approach with a template-based algorithmic approach via a refined
    treatment of exponentiation. Experimental evaluation shows that our algorithmic
    approach is capable of deriving tail bounds that are (i) asymptotically tighter
    than Karp’s method, (ii) match the best-known manually-derived asymptotic tail
    bound for QuickSelect, and (iii) is only slightly worse (with a loglogn factor)
    than the manually-proven optimal asymptotic tail bound for QuickSort. Moreover,
    our algorithmic approach handles all examples (including realistic PRRs such as
    QuickSort, QuickSelect, DiameterComputation, etc.) in less than 0.1 s, showing
    that our approach is efficient in practice."
acknowledgement: We thank Prof. Bican Xia for valuable information on the exponential
  theory of reals. The work is partially supported by the National Natural Science
  Foundation of China (NSFC) with Grant No. 62172271, ERC CoG 863818 (ForM-SMArt),
  the Hong Kong Research Grants Council ECS Project Number 26208122, the HKUST-Kaisa
  Joint Research Institute Project Grant HKJRI3A-055 and the HKUST Startup Grant R9272.
alternative_title:
- LNCS
article_processing_charge: Yes (in subscription journal)
author:
- first_name: Yican
  full_name: Sun, Yican
  last_name: Sun
- first_name: Hongfei
  full_name: Fu, Hongfei
  last_name: Fu
- first_name: Krishnendu
  full_name: Chatterjee, Krishnendu
  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
- first_name: Amir Kafshdar
  full_name: Goharshady, Amir Kafshdar
  id: 391365CE-F248-11E8-B48F-1D18A9856A87
  last_name: Goharshady
  orcid: 0000-0003-1702-6584
citation:
  ama: 'Sun Y, Fu H, Chatterjee K, Goharshady AK. Automated tail bound analysis for probabilistic
    recurrence relations. In: <i>Computer Aided Verification</i>. Vol 13966. Springer
    Nature; 2023:16-39. doi:<a href="https://doi.org/10.1007/978-3-031-37709-9_2">10.1007/978-3-031-37709-9_2</a>'
  apa: 'Sun, Y., Fu, H., Chatterjee, K., &#38; Goharshady, A. K. (2023). Automated
    tail bound analysis for probabilistic recurrence relations. In <i>Computer Aided
    Verification</i> (Vol. 13966, pp. 16–39). Paris, France: Springer Nature. <a href="https://doi.org/10.1007/978-3-031-37709-9_2">https://doi.org/10.1007/978-3-031-37709-9_2</a>'
  chicago: Sun, Yican, Hongfei Fu, Krishnendu Chatterjee, and Amir Kafshdar Goharshady.
    “Automated Tail Bound Analysis for Probabilistic Recurrence Relations.” In <i>Computer
    Aided Verification</i>, 13966:16–39. Springer Nature, 2023. <a href="https://doi.org/10.1007/978-3-031-37709-9_2">https://doi.org/10.1007/978-3-031-37709-9_2</a>.
  ieee: Y. Sun, H. Fu, K. Chatterjee, and A. K. Goharshady, “Automated tail bound
    analysis for probabilistic recurrence relations,” in <i>Computer Aided Verification</i>,
    Paris, France, 2023, vol. 13966, pp. 16–39.
  ista: 'Sun Y, Fu H, Chatterjee K, Goharshady AK. 2023. Automated tail bound analysis
    for probabilistic recurrence relations. Computer Aided Verification. CAV: Computer
    Aided Verification, LNCS, vol. 13966, 16–39.'
  mla: Sun, Yican, et al. “Automated Tail Bound Analysis for Probabilistic Recurrence
    Relations.” <i>Computer Aided Verification</i>, vol. 13966, Springer Nature, 2023,
    pp. 16–39, doi:<a href="https://doi.org/10.1007/978-3-031-37709-9_2">10.1007/978-3-031-37709-9_2</a>.
  short: Y. Sun, H. Fu, K. Chatterjee, A.K. Goharshady, in:, Computer Aided Verification,
    Springer Nature, 2023, pp. 16–39.
conference:
  end_date: 2023-07-22
  location: Paris, France
  name: 'CAV: Computer Aided Verification'
  start_date: 2023-07-17
date_created: 2023-09-10T22:01:12Z
date_published: 2023-07-17T00:00:00Z
date_updated: 2025-09-09T12:55:28Z
day: '17'
ddc:
- '000'
department:
- _id: KrCh
doi: 10.1007/978-3-031-37709-9_2
ec_funded: 1
external_id:
  isi:
  - '001310805600002'
file:
- access_level: open_access
  checksum: 42917e086f8c7699f3bccf84f74fe000
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-20T08:24:47Z
  date_updated: 2023-09-20T08:24:47Z
  file_id: '14348'
  file_name: 2023_LNCS_Sun.pdf
  file_size: 624647
  relation: main_file
  success: 1
file_date_updated: 2023-09-20T08:24:47Z
has_accepted_license: '1'
intvolume: '     13966'
isi: 1
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
page: 16-39
project:
- _id: 0599E47C-7A3F-11EA-A408-12923DDC885E
  call_identifier: H2020
  grant_number: '863818'
  name: 'Formal Methods for Stochastic Models: Algorithms and Applications'
publication: Computer Aided Verification
publication_identifier:
  eissn:
  - 1611-3349
  isbn:
  - '9783031377082'
  issn:
  - 0302-9743
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  link:
  - relation: software
    url: https://github.com/boyvolcano/PRR
scopus_import: '1'
status: public
title: Automated tail bound analysis for probabilistic recurrence relations
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: conference
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 13966
year: '2023'
...
---
_id: '14319'
abstract:
- lang: eng
  text: "We study multigraphs whose edge-sets are the union of three perfect matchings,
    M1, M2, and M3. Given such a graph G and any a1; a2; a3 2 N with a1 +a2 +a3 6
    n - 2, we show there exists a matching M of G with jM \\ Mij = ai for each i 2
    f1; 2; 3g. The bound n - 2 in the theorem is best possible in general. We conjecture
    however that if G is bipartite, the same result holds with n - 2 replaced by n
    - 1. We give a construction that shows such a result would be tight. We\r\nalso
    make a conjecture generalising the Ryser-Brualdi-Stein conjecture with colour\r\nmultiplicities."
acknowledgement: Anastos has received funding from the European Union’s Horizon 2020
  research and in-novation programme under the Marie Sk lodowska-Curie grant agreement
  No 101034413.Fabian’s research is supported by the Deutsche Forschungsgemeinschaft
  (DFG, GermanResearch Foundation) Graduiertenkolleg “Facets of Complexity” (GRK 2434).
article_number: P3.10
article_processing_charge: Yes
article_type: original
arxiv: 1
author:
- first_name: Michael
  full_name: Anastos, Michael
  id: 0b2a4358-bb35-11ec-b7b9-e3279b593dbb
  last_name: Anastos
- first_name: David
  full_name: Fabian, David
  last_name: Fabian
- first_name: Alp
  full_name: Müyesser, Alp
  last_name: Müyesser
- first_name: Tibor
  full_name: Szabó, Tibor
  last_name: Szabó
citation:
  ama: Anastos M, Fabian D, Müyesser A, Szabó T. Splitting matchings and the Ryser-Brualdi-Stein
    conjecture for multisets. <i>Electronic Journal of Combinatorics</i>. 2023;30(3).
    doi:<a href="https://doi.org/10.37236/11714">10.37236/11714</a>
  apa: Anastos, M., Fabian, D., Müyesser, A., &#38; Szabó, T. (2023). Splitting matchings
    and the Ryser-Brualdi-Stein conjecture for multisets. <i>Electronic Journal of
    Combinatorics</i>. Electronic Journal of Combinatorics. <a href="https://doi.org/10.37236/11714">https://doi.org/10.37236/11714</a>
  chicago: Anastos, Michael, David Fabian, Alp Müyesser, and Tibor Szabó. “Splitting
    Matchings and the Ryser-Brualdi-Stein Conjecture for Multisets.” <i>Electronic
    Journal of Combinatorics</i>. Electronic Journal of Combinatorics, 2023. <a href="https://doi.org/10.37236/11714">https://doi.org/10.37236/11714</a>.
  ieee: M. Anastos, D. Fabian, A. Müyesser, and T. Szabó, “Splitting matchings and
    the Ryser-Brualdi-Stein conjecture for multisets,” <i>Electronic Journal of Combinatorics</i>,
    vol. 30, no. 3. Electronic Journal of Combinatorics, 2023.
  ista: Anastos M, Fabian D, Müyesser A, Szabó T. 2023. Splitting matchings and the
    Ryser-Brualdi-Stein conjecture for multisets. Electronic Journal of Combinatorics.
    30(3), P3.10.
  mla: Anastos, Michael, et al. “Splitting Matchings and the Ryser-Brualdi-Stein Conjecture
    for Multisets.” <i>Electronic Journal of Combinatorics</i>, vol. 30, no. 3, P3.10,
    Electronic Journal of Combinatorics, 2023, doi:<a href="https://doi.org/10.37236/11714">10.37236/11714</a>.
  short: M. Anastos, D. Fabian, A. Müyesser, T. Szabó, Electronic Journal of Combinatorics
    30 (2023).
date_created: 2023-09-10T22:01:12Z
date_published: 2023-07-28T00:00:00Z
date_updated: 2025-09-09T12:54:51Z
day: '28'
ddc:
- '510'
department:
- _id: MaKw
doi: 10.37236/11714
ec_funded: 1
external_id:
  arxiv:
  - '2212.03100'
  isi:
  - '001042382200001'
file:
- access_level: open_access
  checksum: 52c46c8cb329f9aaee9ade01525f317b
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-15T08:02:09Z
  date_updated: 2023-09-15T08:02:09Z
  file_id: '14338'
  file_name: 2023_elecJournCombinatorics_Anastos.pdf
  file_size: 247917
  relation: main_file
  success: 1
file_date_updated: 2023-09-15T08:02:09Z
has_accepted_license: '1'
intvolume: '        30'
isi: 1
issue: '3'
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
project:
- _id: fc2ed2f7-9c52-11eb-aca3-c01059dda49c
  call_identifier: H2020
  grant_number: '101034413'
  name: 'IST-BRIDGE: International postdoctoral program'
publication: Electronic Journal of Combinatorics
publication_identifier:
  eissn:
  - 1077-8926
publication_status: published
publisher: Electronic Journal of Combinatorics
quality_controlled: '1'
scopus_import: '1'
status: public
title: Splitting matchings and the Ryser-Brualdi-Stein conjecture for multisets
tmp:
  image: /image/cc_by_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nd/4.0/legalcode
  name: Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0)
  short: CC BY-ND (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 30
year: '2023'
...
---
_id: '14320'
abstract:
- lang: eng
  text: The development of two-dimensional materials has resulted in a diverse range
    of novel, high-quality compounds with increasing complexity. A key requirement
    for a comprehensive quantitative theory is the accurate determination of these
    materials' band structure parameters. However, this task is challenging due to
    the intricate band structures and the indirect nature of experimental probes.
    In this work, we introduce a general framework to derive band structure parameters
    from experimental data using deep neural networks. We applied our method to the
    penetration field capacitance measurement of trilayer graphene, an effective probe
    of its density of states. First, we demonstrate that a trained deep network gives
    accurate predictions for the penetration field capacitance as a function of tight-binding
    parameters. Next, we use the fast and accurate predictions from the trained network
    to automatically determine tight-binding parameters directly from experimental
    data, with extracted parameters being in a good agreement with values in the literature.
    We conclude by discussing potential applications of our method to other materials
    and experimental techniques beyond penetration field capacitance.
acknowledgement: A.F.Y. acknowledges primary support from the Department of Energy
  under award DE-SC0020043, and additional support from the Gordon and Betty Moore
  Foundation under award GBMF9471 for group operations.
article_number: '125411'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Paul M
  full_name: Henderson, Paul M
  id: 13C09E74-18D9-11E9-8878-32CFE5697425
  last_name: Henderson
  orcid: 0000-0002-5198-7445
- first_name: Areg
  full_name: Ghazaryan, Areg
  id: 4AF46FD6-F248-11E8-B48F-1D18A9856A87
  last_name: Ghazaryan
  orcid: 0000-0001-9666-3543
- first_name: Alexander A.
  full_name: Zibrov, Alexander A.
  last_name: Zibrov
- first_name: Andrea F.
  full_name: Young, Andrea F.
  last_name: Young
- first_name: Maksym
  full_name: Serbyn, Maksym
  id: 47809E7E-F248-11E8-B48F-1D18A9856A87
  last_name: Serbyn
  orcid: 0000-0002-2399-5827
citation:
  ama: 'Henderson PM, Ghazaryan A, Zibrov AA, Young AF, Serbyn M. Deep learning extraction
    of band structure parameters from density of states: A case study on trilayer
    graphene. <i>Physical Review B</i>. 2023;108(12). doi:<a href="https://doi.org/10.1103/physrevb.108.125411">10.1103/physrevb.108.125411</a>'
  apa: 'Henderson, P. M., Ghazaryan, A., Zibrov, A. A., Young, A. F., &#38; Serbyn,
    M. (2023). Deep learning extraction of band structure parameters from density
    of states: A case study on trilayer graphene. <i>Physical Review B</i>. American
    Physical Society. <a href="https://doi.org/10.1103/physrevb.108.125411">https://doi.org/10.1103/physrevb.108.125411</a>'
  chicago: 'Henderson, Paul M, Areg Ghazaryan, Alexander A. Zibrov, Andrea F. Young,
    and Maksym Serbyn. “Deep Learning Extraction of Band Structure Parameters from
    Density of States: A Case Study on Trilayer Graphene.” <i>Physical Review B</i>.
    American Physical Society, 2023. <a href="https://doi.org/10.1103/physrevb.108.125411">https://doi.org/10.1103/physrevb.108.125411</a>.'
  ieee: 'P. M. Henderson, A. Ghazaryan, A. A. Zibrov, A. F. Young, and M. Serbyn,
    “Deep learning extraction of band structure parameters from density of states:
    A case study on trilayer graphene,” <i>Physical Review B</i>, vol. 108, no. 12.
    American Physical Society, 2023.'
  ista: 'Henderson PM, Ghazaryan A, Zibrov AA, Young AF, Serbyn M. 2023. Deep learning
    extraction of band structure parameters from density of states: A case study on
    trilayer graphene. Physical Review B. 108(12), 125411.'
  mla: 'Henderson, Paul M., et al. “Deep Learning Extraction of Band Structure Parameters
    from Density of States: A Case Study on Trilayer Graphene.” <i>Physical Review
    B</i>, vol. 108, no. 12, 125411, American Physical Society, 2023, doi:<a href="https://doi.org/10.1103/physrevb.108.125411">10.1103/physrevb.108.125411</a>.'
  short: P.M. Henderson, A. Ghazaryan, A.A. Zibrov, A.F. Young, M. Serbyn, Physical
    Review B 108 (2023).
date_created: 2023-09-12T07:12:12Z
date_published: 2023-09-15T00:00:00Z
date_updated: 2023-09-20T09:38:24Z
day: '15'
department:
- _id: MaSe
- _id: ChLa
- _id: MiLe
doi: 10.1103/physrevb.108.125411
external_id:
  arxiv:
  - '2210.06310'
intvolume: '       108'
issue: '12'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.2210.06310
month: '09'
oa: 1
oa_version: Preprint
publication: Physical Review B
publication_identifier:
  eissn:
  - 2469-9969
  issn:
  - 2469-9950
publication_status: published
publisher: American Physical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Deep learning extraction of band structure parameters from density of states:
  A case study on trilayer graphene'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 108
year: '2023'
...
---
_id: '14321'
abstract:
- lang: eng
  text: We demonstrate the possibility of a coupling between the magnetization direction
    of a ferromagnet and the tilting angle of adsorbed achiral molecules. To illustrate
    the mechanism of the coupling, we analyze a minimal Stoner model that includes
    Rashba spin–orbit coupling due to the electric field on the surface of the ferromagnet.
    The proposed mechanism allows us to study magnetic anisotropy of the system with
    an extended Stoner–Wohlfarth model and argue that adsorbed achiral molecules can
    change magnetocrystalline anisotropy of the substrate. Our research aims to motivate
    further experimental studies of the current-free chirality induced spin selectivity
    effect involving both enantiomers.
acknowledgement: "We thank Zhanybek Alpichshev, Mohammad Reza Safari, Binghai Yan,
  and Yossi Paltiel for enlightening discussions.\r\nM.L. acknowledges support from
  the European Research Council (ERC) Starting Grant No. 801770 (ANGULON). A. C. received
  funding from the European Union’s Horizon Europe research and innovation program
  under the Marie Skłodowska-Curie Grant Agreement No. 101062862 - NeqMolRot."
article_number: '104103'
article_processing_charge: Yes (in subscription journal)
article_type: original
arxiv: 1
author:
- first_name: Ragheed
  full_name: Al Hyder, Ragheed
  id: d1c405be-ae15-11ed-8510-ccf53278162e
  last_name: Al Hyder
- first_name: Alberto
  full_name: Cappellaro, Alberto
  id: 9d13b3cb-30a2-11eb-80dc-f772505e8660
  last_name: Cappellaro
  orcid: 0000-0001-6110-2359
- first_name: Mikhail
  full_name: Lemeshko, Mikhail
  id: 37CB05FA-F248-11E8-B48F-1D18A9856A87
  last_name: Lemeshko
  orcid: 0000-0002-6990-7802
- first_name: Artem
  full_name: Volosniev, Artem
  id: 37D278BC-F248-11E8-B48F-1D18A9856A87
  last_name: Volosniev
  orcid: 0000-0003-0393-5525
citation:
  ama: Al Hyder R, Cappellaro A, Lemeshko M, Volosniev A. Achiral dipoles on a ferromagnet
    can affect its magnetization direction. <i>The Journal of Chemical Physics</i>.
    2023;159(10). doi:<a href="https://doi.org/10.1063/5.0165806">10.1063/5.0165806</a>
  apa: Al Hyder, R., Cappellaro, A., Lemeshko, M., &#38; Volosniev, A. (2023). Achiral
    dipoles on a ferromagnet can affect its magnetization direction. <i>The Journal
    of Chemical Physics</i>. AIP Publishing. <a href="https://doi.org/10.1063/5.0165806">https://doi.org/10.1063/5.0165806</a>
  chicago: Al Hyder, Ragheed, Alberto Cappellaro, Mikhail Lemeshko, and Artem Volosniev.
    “Achiral Dipoles on a Ferromagnet Can Affect Its Magnetization Direction.” <i>The
    Journal of Chemical Physics</i>. AIP Publishing, 2023. <a href="https://doi.org/10.1063/5.0165806">https://doi.org/10.1063/5.0165806</a>.
  ieee: R. Al Hyder, A. Cappellaro, M. Lemeshko, and A. Volosniev, “Achiral dipoles
    on a ferromagnet can affect its magnetization direction,” <i>The Journal of Chemical
    Physics</i>, vol. 159, no. 10. AIP Publishing, 2023.
  ista: Al Hyder R, Cappellaro A, Lemeshko M, Volosniev A. 2023. Achiral dipoles on
    a ferromagnet can affect its magnetization direction. The Journal of Chemical
    Physics. 159(10), 104103.
  mla: Al Hyder, Ragheed, et al. “Achiral Dipoles on a Ferromagnet Can Affect Its
    Magnetization Direction.” <i>The Journal of Chemical Physics</i>, vol. 159, no.
    10, 104103, AIP Publishing, 2023, doi:<a href="https://doi.org/10.1063/5.0165806">10.1063/5.0165806</a>.
  short: R. Al Hyder, A. Cappellaro, M. Lemeshko, A. Volosniev, The Journal of Chemical
    Physics 159 (2023).
corr_author: '1'
date_created: 2023-09-13T09:25:09Z
date_published: 2023-09-11T00:00:00Z
date_updated: 2025-09-09T12:57:42Z
day: '11'
ddc:
- '530'
department:
- _id: MiLe
doi: 10.1063/5.0165806
ec_funded: 1
external_id:
  arxiv:
  - '2306.17592'
  isi:
  - '001133333600011'
  pmid:
  - '37694742'
file:
- access_level: open_access
  checksum: 507ab65ab29e2c987c94cabad7c5370b
  content_type: application/pdf
  creator: acappell
  date_created: 2023-09-13T09:34:20Z
  date_updated: 2023-09-13T09:34:20Z
  file_id: '14322'
  file_name: 104103_1_5.0165806.pdf
  file_size: 5749653
  relation: main_file
  success: 1
file_date_updated: 2023-09-13T09:34:20Z
has_accepted_license: '1'
intvolume: '       159'
isi: 1
issue: '10'
keyword:
- Physical and Theoretical Chemistry
- General Physics and Astronomy
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: bd7b5202-d553-11ed-ba76-9b1c1b258338
  grant_number: '101062862'
  name: Non-Equilibrium Field Theory of Molecular Rotations
- _id: 2688CF98-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '801770'
  name: 'Angulon: physics and applications of a new quasiparticle'
publication: The Journal of Chemical Physics
publication_identifier:
  eissn:
  - 1089-7690
  issn:
  - 0021-9606
publication_status: published
publisher: AIP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Achiral dipoles on a ferromagnet can affect its magnetization direction
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 159
year: '2023'
...
